If you made any changes in Pure these will be visible here soon.

Research Output 2006 2019

  • 131 Article
  • 4 Chapter
  • 4 Research VU University Amsterdam, graduation VU University Amsterdam
  • 1 Research external, graduation VU University Amsterdam
2019

Clinical, biochemical, and molecular overview of transaldolase deficiency and evaluation of the endocrine function: update of 34 patients

Williams, M., Valayannopoulos, V., Altassan, R., Chung, W. K., Heijboer, A. C., Keng, W. T., Lapatto, R., McClean, P., Mulder, M. F., Tylki-Szymańska, A., Walenkamp, M-J. E., Alfadhel, M., Alakeel, H., Salomons, G. S., Eyaid, W. & Wamelink, M. M. C., 2019, In : Journal of Inherited Metabolic Disease. 42, 1, p. 147-158

Research output: Contribution to journalArticleAcademicpeer-review

Open Access

D-2-hydroxyglutaric aciduria Type I: Functional analysis of D2HGDH missense variants

Pop, A., Struys, E. A., Jansen, E. E. W., Fernandez, M. R., Kanhai, W. A., van Dooren, S. J. M., Ozturk, S., van Oostendorp, J., Lennertz, P., Kranendijk, M., van der Knaap, M. S., Gibson, K. M., van Schaftingen, E. & Salomons, G. S., 2019, In : Human Mutation.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access

Maternal glutamine supplementation in murine succinic semialdehyde dehydrogenase deficiency, a disorder of γ-aminobutyric acid metabolism

Brown, M. N., Walters, D. C., Schmidt, M. A., Hill, J., McConnell, A., Jansen, E. E. W., Salomons, G. S., Arning, E., Bottiglieri, T., Gibson, K. M. & Roullet, J-B., 2019, In : Journal of Inherited Metabolic Disease. 42, 5, p. 1030-1039

Research output: Contribution to journalArticleAcademicpeer-review

2018

An overview of combined D-2- and L-2-hydroxyglutaric aciduria: functional analysis of CIC variants

Pop, A., Williams, M., Struys, E. A., Monné, M., Jansen, E. E. W., de Grassi, A., Kanhai, W. A., Scarcia, P., Ojeda, M. R. F., Porcelli, V., van Dooren, S. J. M., Lennertz, P., Nota, B., Abdenur, J. E., Coman, D., Das, A. M., El-Gharbawy, A., Nuoffer, J. M., Polic, B., Santer, R. & 5 othersWeinhold, N., Zuccarelli, B., Palmieri, F., Palmieri, L. & Salomons, G. S., 1 Mar 2018, In : Journal of Inherited Metabolic Disease. 41, 2, p. 169-180 12 p.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access

Bi-allelic Mutations in EPRS, Encoding the Glutamyl-Prolyl-Aminoacyl-tRNA Synthetase, Cause a Hypomyelinating Leukodystrophy

Mendes, M. I., Salazar, M. G., Guerrero, K., Thiffault, I., Salomons, G. S., Gauquelin, L., Tran, L. T., Forget, D., Gauthier, M-S., Waisfisz, Q., Smith, D. E. C., Simons, C., van der Knaap, M. S., Marquardt, I., Lemes, A., Mierzewska, H., Weschke, B., Koehler, W., Coulombe, B., Wolf, N. I. & 1 othersBernard, G., 5 Apr 2018, In : American journal of human genetics. 102, 4, p. 676-684

Research output: Contribution to journalArticleAcademicpeer-review

Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease

Kamps, R., Szklarczyk, R., Theunissen, T. E., Hellebrekers, D. M. E. I., Sallevelt, S. C. E. H., Boesten, I. B., de Koning, B., van den Bosch, B. J., Salomons, G. S., Simas-Mendes, M., Verdijk, R., Schoonderwoerd, K., de Coo, I. F. M., Vanoevelen, J. M. & Smeets, H. J. M., 2018, In : European Journal of Human Genetics. 26, 4, p. 537-551

Research output: Contribution to journalArticleAcademicpeer-review

Idh1-mutated transgenic zebrafish lines: An in-vivo model for drug screening and functional analysis

Gao, Y., de Wit, M., Struys, E. A., van der Linde, H. C. Z., Salomons, G. S., Lamfers, M. L. M., Willemsen, R., Sillevis Smitt, P. A. E. & French, P. J., 2018, In : PLoS ONE. 13, 6, e0199737.

Research output: Contribution to journalArticleAcademicpeer-review

Open Access

The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: A common epileptic encephalopathy

Coughlin, C. R., Swanson, M. A., Spector, E., Meeks, N. J. L., Kronquist, K. E., Aslamy, M., Wempe, M. F., van Karnebeek, C. D. M., Gospe, S. M., Aziz, V. G., Tsai, B. P., Gao, H., Nagy, P. L., Hyland, K., van Dooren, S. J. M., Salomons, G. S. & van Hove, J. L. K., 2018, In : Journal of Inherited Metabolic Disease.

Research output: Contribution to journalArticleAcademicpeer-review

Treatment outcome of creatine transporter deficiency: international retrospective cohort study

Bruun, T. U. J., Sidky, S., Bandeira, A. O., Debray, F-G., Ficicioglu, C., Goldstein, J., Joost, K., Koeberl, D. D., Luísa, D., Nassogne, M-C., O’Sullivan, S., Õunap, K., Schulze, A., van Maldergem, L., Salomons, G. S. & Mercimek-Andrews, S., 2018, In : METABOLIC BRAIN DISEASE. 33, 3, p. 875-884

Research output: Contribution to journalArticleAcademicpeer-review

Treatment outcome of twenty-two patients with guanidinoacetate methyltransferase deficiency: An international retrospective cohort study

Khaikin, Y., Sidky, S., Abdenur, J., Anastasi, A., Ballhausen, D., Buoni, S., Chan, A., Cheillan, D., Dorison, N., Goldenberg, A., Goldstein, J., Hofstede, F. C., Jacquemont, M-L., Koeberl, D. D., Lion-Francois, L., Lund, A. M., Mention, K., Mundy, H., O'Rourke, D., Pitelet, G. & 6 othersRaspall-Chaure, M., Tassini, M., Billette de Villemeur, T., Williams, M., Salomons, G. S. & Mercimek-Andrews, S., 2018, In : European Journal of Paediatric Neurology. 22, 3, p. 369-379

Research output: Contribution to journalArticleAcademicpeer-review

2017

Characterization of the first knock-out aldh7a1 zebrafish model for pyridoxine-dependent epilepsy using CRISPR-Cas9 technology

Zabinyakov, N., Bullivant, G., Cao, F., Fernandez Ojeda, M., Jia, Z. P., Wen, X. Y., Dowling, J. J., Salomons, G. S. & Mercimek-Andrews, S., 1 Oct 2017, In : PLoS ONE. 12, 10, e0186645.

Research output: Contribution to journalArticleAcademicpeer-review

Clinically Distinct Phenotypes of Canavan Disease Correlate with Residual Aspartoacylase Enzyme Activity

Mendes, M. I., Smith, D. E. C., Pop, A., Lennertz, P., Fernandez Ojeda, M. R., Kanhai, W. A., van Dooren, S. J. M., Anikster, Y., Barić, I., Boelen, C., Campistol, J., de Boer, L., Kariminejad, A., Kayserili, H., Roubertie, A., Verbruggen, K. T., Vianey-Saban, C., Williams, M. & Salomons, G. S., 1 May 2017, In : Human Mutation. 38, 5, p. 524-531 8 p.

Research output: Contribution to journalArticleAcademicpeer-review

In vitro modeling of experimental succinic semialdehyde dehydrogenase deficiency (SSADHD) using brain-derived neural stem cells

Vogel, K. R., Ainslie, G. R., Jansen, E. E., Salomons, G. S., Roullet, J. B. & Gibson, K. M., 1 Oct 2017, In : PLoS ONE. 12, 10, e0186919.

Research output: Contribution to journalArticleAcademicpeer-review

Propionic acidemia as a cause of adult-onset dilated cardiomyopathy

Riemersma, M., Hazebroek, M. R., Helderman-Van Den Enden, A. T. J. M., Salomons, G. S., Ferdinandusse, S., Brouwers, M. C. G. J., Van Der Ploeg, L., Heymans, S., Glatz, J. F. C., Van Den Wijngaard, A., Krapels, I. P. C., Bierau, J. & Brunner, H. G., 1 Nov 2017, In : European Journal of Human Genetics. 25, 11, p. 1195-1201 7 p.

Research output: Contribution to journalArticleAcademicpeer-review

Punctate white matter lesions in full-term infants with neonatal seizures associated with SLC13A5 mutations

Weeke, L. C., Brilstra, E., Braun, K. P., Zonneveld-Huijssoon, E., Salomons, G. S., Koeleman, B. P., van Gassen, K. L., van Straaten, H. L., Craiu, D. & de Vries, L. S., Mar 2017, In : European Journal of Paediatric Neurology. 21, 2, p. 396-403 8 p.

Research output: Contribution to journalArticleAcademicpeer-review

Targeted screening of succinic semialdehyde dehydrogenase deficiency (SSADHD) employing an enzymatic assay for γ-hydroxybutyric acid (GHB) in biofluids

Wernli, C., Finochiaro, S., Volken, C., Andresen-Streichert, H., Buettler, A., Gygax, D., Salomons, G. S., Jansen, E. E., Ainslie, G. R., Vogel, K. R. & Gibson, K. M., 1 Jun 2017, In : Molecular Genetics and Metabolism Reports. 11, p. 81-89 9 p.

Research output: Contribution to journalArticleAcademicpeer-review

The acute effect of beta-guanidinopropionic acid versus creatine or placebo in healthy men (ABC-Trial): A randomized controlled first-in-human trial

Karamat, F. A., Horjus, D. L., Haan, Y. C., van der Woude, L., Schaap, M. C., Oudman, I., van Montfrans, G. A., Nieuwland, R., Salomons, G. S., Clark, J. F. & Brewster, L. M., 1 Dec 2017, In : British Journal of Clinical Pharmacology. 83, 12, p. 2626-2635 10 p.

Research output: Contribution to journalArticleAcademicpeer-review

Therapeutic relevance of mTOR inhibition in murine succinate semialdehyde dehydrogenase deficiency (SSADHD), a disorder of GABA metabolism

Vogel, K. R., Ainslie, G. R., Jansen, E. E. W., Salomons, G. S. & Gibson, K. M., 1 Jan 2017, In : Biochimica et Biophysica Acta - Molecular Basis of Disease. 1863, 1, p. 33-42 10 p.

Research output: Contribution to journalArticleAcademicpeer-review

2016

2-hydroxyglutaric aciduria

Struys, EA., van der Knaap, MS. & Salomons, GS., 18 Aug 2016, Inherited Metabolic Disease in Adults: A Clinical Guide. Hollak, CEM. & Lachmann, R. (eds.). Oxford University Press, Chapter 22

Research output: Chapter in Book/Report/Conference proceedingChapterAcademic

Absent Thalami Caused by a Homozygous EARS2 Mutation: Expanding Disease Spectrum of LTBL

Kevelam, S. H., Klouwer, F. C. C., Fock, J. M., Salomons, G. S., Bugiani, M. & van der Knaap, M. S., Jan 2016, In : Neuropediatrics. 47, 1, p. 64-67

Research output: Contribution to journalArticleAcademicpeer-review

Alexander disease - astrogliopathy considered as leukodystrophy - experience of an institution

Mierzewska, H., Mierzewska-Schmidt, M., Salomons, G. S., Dudzińska, M. & Szczepanik, E., 1 Apr 2016, In : Developmental period medicine. 20, 2, p. 110-117 8 p.

Research output: Contribution to journalArticleAcademicpeer-review

A pilot study to estimate incidence of guanidinoacetate methyltransferase deficiency in newborns by direct sequencing of the GAMT gene

Mercimek-Mahmutoglu, S., Pop, A., Kanhai, W., Ojeda, M. F., Holwerda, U., Smith, D. E. C., Loeber, J. G., Schielen, P. C. J. I. & Salomons, G. S., 1 Jan 2016, In : Gene. 575, 1, p. 127-131

Research output: Contribution to journalArticleAcademicpeer-review

A small molecule inhibitor of mutant IDH2 rescues cardiomyopathy in a D-2-hydroxyglutaric aciduria type II mouse model

Wang, F., Travins, J., Lin, Z., Si, Y., Chen, Y., Powe, J., Murray, S., Zhu, D., Artin, E., Gross, S., Santiago, S., Steadman, M., Kernytsky, A., Straley, K., Lu, C., Pop, A., Struys, E. A., Jansen, E. E. W., Salomons, G. S., David, M. D. & 14 othersQuivoron, C., Penard-Lacronique, V., Regan, K. S., Liu, W., Dang, L., Yang, H., Silverman, L., Agresta, S., Dorsch, M., Biller, S., Yen, K., Cang, Y., Su, S. S. M. & Jin, S., 1 Nov 2016, In : Journal of Inherited Metabolic Disease. 39, 6, p. 807-820 14 p.

Research output: Contribution to journalArticleAcademicpeer-review

Correlation of blood biomarkers with age informs pathomechanisms in succinic semialdehyde dehydrogenase deficiency (SSADHD), a disorder of GABA metabolism

Jansen, E. E., Vogel, K. R., Salomons, G. S., Pearl, P. L., Roullet, J. B. & Gibson, K. M., 1 Nov 2016, In : Journal of Inherited Metabolic Disease. 39, 6, p. 795-800 6 p.

Research output: Contribution to journalArticleAcademicpeer-review

Creatine deficiency syndromes

Stöckler-Isiroglu, S., Mercimek-Mahmutoglu, S. & Salomons, GS., 2016, Metabolic Diseases: Diagnosis and Treatment. Saudubray, J. M., Baumgartner, M. & Walter, J. H. (eds.). 6 ed. Heidelberg, Berlin, Germany: Springer-Verlag Berlin Heidelberg, p. 243-248

Research output: Chapter in Book/Report/Conference proceedingChapterAcademic

Creatine Transporter Deficiency: Screening of Males with Neurodevelopmental Disorders and Neurocognitive Characterization of a Case

Thurm, A., Himelstein, D., D'Souza, P., Rennert, O., Jiang, S., Olatunji, D., Longo, N., Pasquali, M., Swedo, S., Salomons, G. S. & Carrillo, N., May 2016, In : Journal of Developmental and Behavioral Pediatrics. 37, 4, p. 322-326

Research output: Contribution to journalArticleAcademicpeer-review

Frequent reconstitution of IDH2(R140Q) mutant clonal multilineage hematopoiesis following chemotherapy for acute myeloid leukemia

Wiseman, D. H., Williams, E. L., Wilks, D. P., Sun Leong, H., Somerville, T. D. D., Dennis, M. W., Struys, E. A., Bakkali, A., Salomons, G. S. & Somervaille, T. C. P., Sep 2016, In : Leukemia. 30, 9, p. 1946-1950 5 p.

Research output: Contribution to journalArticleAcademicpeer-review

Gallbladder and the risk of polyps and carcinoma in metachromatic leukodystrophy

van Rappard, D. F., Bugiani, M., Boelens, J. J., van der Steeg, A., Daams, F., de Meij, T. G. J., van Doorn, M. M. A. C., van Hasselt, P. M., Gouma, D. J., Verbeke, J. I. M. L., Hollak, C. E. M., van Hecke, W., Salomons, G. S., van der Knaap, M. & Wolf, N. I., 5 Jul 2016, In : Neurology. 87, 1, p. 103-111

Research output: Contribution to journalArticleAcademicpeer-review

Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects

Boyle, L., Wamelink, M. M. C., Salomons, G. S., Roos, B., Pop, A., Dauber, A., Hwa, V., Andrew, M., Douglas, J., Feingold, M., Kramer, N., Saitta, S., Retterer, K., Cho, M. T., Begtrup, A., Monaghan, K. G., Wynn, J. & Chung, W. K., 2 Jun 2016, In : American journal of human genetics. 98, 6, p. 1235-1242

Research output: Contribution to journalArticleAcademicpeer-review

Phenotyping GABA transaminase deficiency: a case description and literature review

Louro, P., Ramos, L., Robalo, C., Cancelinha, C., Dinis, A., Veiga, R., Pina, R., Rebelo, O., Pop, A., Diogo, L., Salomons, G. S. & Garcia, P., Sep 2016, In : Journal of Inherited Metabolic Disease. 39, 5, p. 743-747

Research output: Contribution to journalArticleAcademicpeer-review

Pyridoxine responsive epilepsy caused by a novel homozygous PNPO mutation

Jaeger, B., Abeling, N. G., Salomons, G. S., Struys, E. A., Simas-Mendes, M., Geukers, V. G. & Poll-The, B. T., 1 Mar 2016, In : Molecular Genetics and Metabolism Reports. 6, p. 60-63 4 p.

Research output: Contribution to journalArticleAcademicpeer-review

2015

Carrier frequency of guanidinoacetate methyltransferase deficiency in the general population by functional characterization of missense variants in the GAMT gene

Desroches, C. L., Patel, J., Wang, P. X., Minassian, B., Marshall, C. R., Salomons, G. & Mercimek-Mahmutoglu, S., 2015, In : Molecular Genetics and Genomics. 290, 6, p. 2163-2171

Research output: Contribution to journalArticleAcademicpeer-review

Continuous Age- and Sex-Adjusted Reference Intervals of Urinary Markers for Cerebral Creatine Deficiency Syndromes: A Novel Approach to the Definition of Reference Intervals

Morkrid, L., Rowe, A. D., Elgstoen, K. B. P., Olesen, J. H., Ruijter, G., Hall, P. L., Tortorelli, S., Schulze, A., Kyriakopoulou, L., Wamelink, M. M. C., van de Kamp, J. M., Salomons, G. S. & Rinaldo, P., 2015, In : Clinical Chemistry. 61, 5, p. 760-768

Research output: Contribution to journalArticleAcademicpeer-review

Creatine Deficiency Syndromes

Mahmutoglu, S. & Salomons, G. S., 2015, GeneReviews® [internet]. Seattle (WA): University of Washington

Research output: Chapter in Book/Report/Conference proceedingChapterAcademic

Direct comparison of quantitative digital PCR and 2-hydroxyglutarate enantiomeric ratio for IDH mutant allele frequency assessment in myeloid malignancy

Wiseman, D. H., Struys, E. A., Wilks, D. P., Clark, C. I., Dennis, M. W., Jansen, E. E. W., Salomons, G. & Somervaille, T. C. P., 2015, In : Leukemia. 29, 12, p. 2421-2423

Research output: Contribution to journalArticleAcademicpeer-review

Estimated carrier frequency of creatine transporter deficiency in females in the general population using functional characterization of novel missense variants in the SLC6A8 gene

Desroches, C. L., Patel, J., Wang, P. X., Minassian, B., Salomons, G., Marshall, C. R. & Mercimek-Mahmutoglu, S., 2015, In : Gene. 565, 2, p. 187-191

Research output: Contribution to journalArticleAcademicpeer-review

Expanding the Clinical Spectrum of Mitochondrial Citrate Carrier (SLC25A1) Deficiency: Facial Dysmorphism in Siblings with Epileptic Encephalopathy and Combined D,L-2-Hydroxyglutaric Aciduria

Prasun, P., Young, S., Salomons, G., Werneke, A., Jiang, Y. H., Struijs, E. A., Paige, M., Avantaggiati, M. L. & McDonald, M., 2015, In : JIMD Reports. 19, p. 111-115

Research output: Contribution to journalArticleAcademicpeer-review

First two unrelated cases of isolated sedoheptulokinase deficiency: A benign disorder?

Wamelink, M. M. C., Ramos, R. J. J. F., van den Elzen, A. P. M., Ruijter, G. J. G., Bonte, R., Diogo, L., Garcia, P., Neves, N., Nota, B., Haschemi, A., de Almeida, I. T. & Salomons, G., 2015, In : Journal of Inherited Metabolic Disease. 38, 5, p. 889-894

Research output: Contribution to journalArticleAcademicpeer-review

Genotype-phenotype correlation of contiguous gene deletions of SLC6A8, BCAP31 and ABCD1

van de Kamp, J. M., Errami, A., Howidi, M., Anselm, I., Winter, S., Phalin-Roque, J., Osaka, H., van Dooren, S. J. M., Mancini, G. M., Steinberg, S. J. & Salomons, G., 2015, In : Clinical Genetics. 87, 2, p. 141-147

Research output: Contribution to journalArticleAcademicpeer-review

Inhibition of mutant IDH1 decreases D-2-HG levels without affecting tumorigenic properties of chondrosarcoma cell lines

Suijker, J., Oosting, J., Koornneef, A., Struys, E. A., Salomons, G., Schaap, F. G., Waaijer, C. J. F., Wijers-Koster, P. M., Bruijn, I. H. B. D., Haazen, L., Riester, S. M., Dudakovic, A., Danen, E., Cleton-Jansen, A. M., van Wijnen, A. J. & Bovee, J. V. M. G., 2015, In : Oncotarget. 6, 14, p. 12505-12519

Research output: Contribution to journalArticleAcademicpeer-review

Natural history of succinic semialdehyde dehydrogenase deficiency through adulthood

Lapalme-Remis, S., Lewis, E. C., De Meulemeester, C., Chakraborty, P., Gibson, K. M., Torres, C., Guberman, A., Salomons, G., Jakobs, C., Ali-Ridha, A., Parviz, M. & Pearl, P. L., 2015, In : Neurology. 85, 10, p. 861-865

Research output: Contribution to journalArticleAcademicpeer-review

Recessive ITPA Mutations Cause an Early Infantile Encephalopathy

Kevelam, S. H., Bierau, J., Salvarinova, R., Agrawal, S., Honzik, T., Visser, D., Weiss, M. M., Salomons, G., Abbink, T. E. M., Waisfisz, Q. & van der Knaap, M. S., 2015, In : Annals of Neurology. 78, 4, p. 649-658

Research output: Contribution to journalArticleAcademicpeer-review

Small aminothiol compounds improve the function of Arg to Cys variant proteins: effect on the human cystathionine beta-synthase p.R336C

Mendes, M. I. S., Smith, D. E. C., Vicente, J. B., Tavares de Almeida, I., Ben-Omran, T., Salomons, G., Rivera, I. A., Leandro, P. & Blom, H. J., 2015, In : Human Molecular Genetics. 24, 25, p. 7339-7348

Research output: Contribution to journalArticleAcademicpeer-review

Torin 1 partially corrects vigabatrin-induced mitochondrial increase in mouse

Vogel, K. R., Ainslie, G. R., Jansen, E. E. W., Salomons, G. & Gibson, K. M., 2015, In : Annals of Clinical and Translational Neurology. 2, 6, p. 699-706

Research output: Contribution to journalArticleAcademicpeer-review

2014

Case Study for the Evaluation of Current Treatment Recommendations of Guanidinoacetate Methyltransferase Deficiency: Ineffectiveness of Sodium Benzoate

Mercimek-Mahmutoglu, S., Salomons, G. S. & Chan, A., 2014, In : Pediatric Neurology. 51, 1, p. 133-137

Research output: Contribution to journalArticleAcademicpeer-review

Clinical and molecular characteristics of two transaldolase-deficient patients

Tylki-Szymanska, A., Wamelink, M. M. C., Stradomska, T. J., Salomons, G. S., Taybert, J., Dabrowska-Leonik, N. & Rurarz, M., 2014, In : European Journal of Pediatrics. 173, 12, p. 1679-1682

Research output: Contribution to journalArticleAcademicpeer-review

Cloning and characterization of the promoter regions from the parent and paralogobs creatine transporter genes

Ndika, J. D. T., Lusink, V., Beaubrun, C., Kanhai, W., Martinez-Munoz, C., Jakobs, C. A. J. M. & Salomons, G. S., 2014, In : Gene. 533, 2, p. 488-493

Research output: Contribution to journalArticleAcademicpeer-review

Combined D2-/L2-hydroxyglutaric aciduria (SLC25A1 deficiency): clinical course and effects of citrate treatment

Muhlhausen, C., Salomons, G. S., Lukacs, Z., Struys, E. A., van der Knaap, M. S., Ullrich, K. & Santer, R., 2014, In : Journal of Inherited Metabolic Disease. 37, 5, p. 775-781

Research output: Contribution to journalArticleAcademicpeer-review

32 Downloads (Pure)

Creatine Deficiency Syndromes: A Clinical, Molecular and Functional Approach

Ndika, J. D. T., 2014

Research output: ThesisResearch VU University Amsterdam, graduation VU University AmsterdamAcademic

File
39 Downloads (Pure)

Creatine Transporter Deficiency: How to get from A to CTG

Betsalel, O. T., 2014

Research output: ThesisResearch VU University Amsterdam, graduation VU University AmsterdamAcademic

File