Erratum: Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome (The American Journal of Human Genetics (2018) 103(3) (431–439), (S0002929718302374), (10.1016/j.ajhg.2018.07.010))

Shereen G. Ghosh; Kerstin Becker; He Huang; Tracy D. Salazar; Guoliang Chai; Vincenzo Salpietro; Lihadh Al-Gazali; Quinten Waisfisz; Haicui Wang; Keith K. Vaux; Valentina Stanley; Andreea Manole; Ugur Akpulat; Marjan M. Weiss; Stephanie Efthymiou; Michael G. Hanna; Carlo Minetti; Pasquale Striano; Livia Pisciotta; Elisa De Grandis; Janine Altmüller; Lisa Weixler; Peter Nürnberg; Holger Thiele; Uluc Yis; Tuncay Derya Okur; Ayse Ipek Polat; Nafise Amiri; Mohammad Doosti; Ehsan Ghayoor Karimani; Mehran B. Toosi; Gabriel Haddad; Mert Karakaya; Brunhilde Wirth; Johanna M. van Hagen; Nicole I. Wolf; Reza Maroofian; Henry Houlden; Sebahattin Cirak; Joseph G. Gleeson

doi:10.1016/j.ajhg.2021.11.013

Erratum: Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome (The American Journal of Human Genetics (2018) 103(3) (431–439), (S0002929718302374), (10.1016/j.ajhg.2018.07.010))

Shereen G. Ghosh, Kerstin Becker, He Huang, Tracy D. Salazar, Guoliang Chai, Vincenzo Salpietro, Lihadh Al-Gazali, Quinten Waisfisz, Haicui Wang, Keith K. Vaux, Valentina Stanley, Andreea Manole, Ugur Akpulat, Marjan M. Weiss, Stephanie Efthymiou, Michael G. Hanna, Carlo Minetti, Pasquale Striano, Livia Pisciotta, Elisa De GrandisJanine Altmüller, Lisa Weixler, Peter Nürnberg, Holger Thiele, Uluc Yis, Tuncay Derya Okur, Ayse Ipek Polat, Nafise Amiri, Mohammad Doosti, Ehsan Ghayoor Karimani, Mehran B. Toosi, Gabriel Haddad, Mert Karakaya, Brunhilde Wirth, Johanna M. van Hagen, Nicole I. Wolf, Reza Maroofian, Henry Houlden, Sebahattin Cirak^*, Joseph G. Gleeson

^*Corresponding author for this work

Research output: Contribution to journal › Comment/Letter to the editor › Academic

Abstract

(The American Journal of Human Genetics 103, 431–439; September 6, 2018) Lisa Weixler has been added to the author list for her experimental and scientific contributions to the biophysical analysis of wild-type and mutant proteins. Her contributions were already mentioned in the acknowledgments. The authors apologize for initially only listing her in the acknowledgments and for the inconvenience. The author list has been corrected online and appears correctly here, and Lisa Weixler's affiliation is indicated as footnote 3: Center for Molecular Medicine Cologne, Cologne, Germany.

Original language	English
Pages (from-to)	2385
Number of pages	1
Journal	American journal of human genetics
Volume	108
Issue number	12
DOIs	https://doi.org/10.1016/j.ajhg.2021.11.013
Publication status	Published - 2 Dec 2021

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10.1016/j.ajhg.2021.11.013

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Ghosh, S. G., Becker, K., Huang, H., Salazar, T. D., Chai, G., Salpietro, V., Al-Gazali, L., Waisfisz, Q., Wang, H., Vaux, K. K., Stanley, V., Manole, A., Akpulat, U., Weiss, M. M., Efthymiou, S., Hanna, M. G., Minetti, C., Striano, P., Pisciotta, L., ... Gleeson, J. G. (2021). Erratum: Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome (The American Journal of Human Genetics (2018) 103(3) (431–439), (S0002929718302374), (10.1016/j.ajhg.2018.07.010)). American journal of human genetics, 108(12), 2385. https://doi.org/10.1016/j.ajhg.2021.11.013

Ghosh, Shereen G. ; Becker, Kerstin ; Huang, He et al. / Erratum : Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome (The American Journal of Human Genetics (2018) 103(3) (431–439), (S0002929718302374), (10.1016/j.ajhg.2018.07.010)). In: American journal of human genetics. 2021 ; Vol. 108, No. 12. pp. 2385.

@article{fd026b05241846f0aba818fb4b7a3570,

title = "Erratum: Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome (The American Journal of Human Genetics (2018) 103(3) (431–439), (S0002929718302374), (10.1016/j.ajhg.2018.07.010))",

abstract = "(The American Journal of Human Genetics 103, 431–439; September 6, 2018) Lisa Weixler has been added to the author list for her experimental and scientific contributions to the biophysical analysis of wild-type and mutant proteins. Her contributions were already mentioned in the acknowledgments. The authors apologize for initially only listing her in the acknowledgments and for the inconvenience. The author list has been corrected online and appears correctly here, and Lisa Weixler's affiliation is indicated as footnote 3: Center for Molecular Medicine Cologne, Cologne, Germany.",

author = "Ghosh, {Shereen G.} and Kerstin Becker and He Huang and Salazar, {Tracy D.} and Guoliang Chai and Vincenzo Salpietro and Lihadh Al-Gazali and Quinten Waisfisz and Haicui Wang and Vaux, {Keith K.} and Valentina Stanley and Andreea Manole and Ugur Akpulat and Weiss, {Marjan M.} and Stephanie Efthymiou and Hanna, {Michael G.} and Carlo Minetti and Pasquale Striano and Livia Pisciotta and {De Grandis}, Elisa and Janine Altm{\"u}ller and Lisa Weixler and Peter N{\"u}rnberg and Holger Thiele and Uluc Yis and Okur, {Tuncay Derya} and Polat, {Ayse Ipek} and Nafise Amiri and Mohammad Doosti and Karimani, {Ehsan Ghayoor} and Toosi, {Mehran B.} and Gabriel Haddad and Mert Karakaya and Brunhilde Wirth and {van Hagen}, {Johanna M.} and Wolf, {Nicole I.} and Reza Maroofian and Henry Houlden and Sebahattin Cirak and Gleeson, {Joseph G.}",

note = "Publisher Copyright: {\textcopyright} 2018",

year = "2021",

month = dec,

day = "2",

doi = "10.1016/j.ajhg.2021.11.013",

language = "English",

volume = "108",

pages = "2385",

journal = "American journal of human genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "12",

}

Ghosh, SG, Becker, K, Huang, H, Salazar, TD, Chai, G, Salpietro, V, Al-Gazali, L, Waisfisz, Q, Wang, H, Vaux, KK, Stanley, V, Manole, A, Akpulat, U, Weiss, MM, Efthymiou, S, Hanna, MG, Minetti, C, Striano, P, Pisciotta, L, De Grandis, E, Altmüller, J, Weixler, L, Nürnberg, P, Thiele, H, Yis, U, Okur, TD, Polat, AI, Amiri, N, Doosti, M, Karimani, EG, Toosi, MB, Haddad, G, Karakaya, M, Wirth, B, van Hagen, JM , Wolf, NI, Maroofian, R, Houlden, H, Cirak, S & Gleeson, JG 2021, 'Erratum: Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome (The American Journal of Human Genetics (2018) 103(3) (431–439), (S0002929718302374), (10.1016/j.ajhg.2018.07.010))', American journal of human genetics, vol. 108, no. 12, pp. 2385. https://doi.org/10.1016/j.ajhg.2021.11.013

Erratum: Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome (The American Journal of Human Genetics (2018) 103(3) (431–439), (S0002929718302374), (10.1016/j.ajhg.2018.07.010)). / Ghosh, Shereen G.; Becker, Kerstin; Huang, He et al.
In: American journal of human genetics, Vol. 108, No. 12, 02.12.2021, p. 2385.

Research output: Contribution to journal › Comment/Letter to the editor › Academic

TY - JOUR

T1 - Erratum

T2 - Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome (The American Journal of Human Genetics (2018) 103(3) (431–439), (S0002929718302374), (10.1016/j.ajhg.2018.07.010))

AU - Ghosh, Shereen G.

AU - Becker, Kerstin

AU - Huang, He

AU - Salazar, Tracy D.

AU - Chai, Guoliang

AU - Salpietro, Vincenzo

AU - Al-Gazali, Lihadh

AU - Waisfisz, Quinten

AU - Wang, Haicui

AU - Vaux, Keith K.

AU - Stanley, Valentina

AU - Manole, Andreea

AU - Akpulat, Ugur

AU - Weiss, Marjan M.

AU - Efthymiou, Stephanie

AU - Hanna, Michael G.

AU - Minetti, Carlo

AU - Striano, Pasquale

AU - Pisciotta, Livia

AU - De Grandis, Elisa

AU - Altmüller, Janine

AU - Weixler, Lisa

AU - Nürnberg, Peter

AU - Thiele, Holger

AU - Yis, Uluc

AU - Okur, Tuncay Derya

AU - Polat, Ayse Ipek

AU - Amiri, Nafise

AU - Doosti, Mohammad

AU - Karimani, Ehsan Ghayoor

AU - Toosi, Mehran B.

AU - Haddad, Gabriel

AU - Karakaya, Mert

AU - Wirth, Brunhilde

AU - van Hagen, Johanna M.

AU - Wolf, Nicole I.

AU - Maroofian, Reza

AU - Houlden, Henry

AU - Cirak, Sebahattin

AU - Gleeson, Joseph G.

PY - 2021/12/2

Y1 - 2021/12/2

N2 - (The American Journal of Human Genetics 103, 431–439; September 6, 2018) Lisa Weixler has been added to the author list for her experimental and scientific contributions to the biophysical analysis of wild-type and mutant proteins. Her contributions were already mentioned in the acknowledgments. The authors apologize for initially only listing her in the acknowledgments and for the inconvenience. The author list has been corrected online and appears correctly here, and Lisa Weixler's affiliation is indicated as footnote 3: Center for Molecular Medicine Cologne, Cologne, Germany.

AB - (The American Journal of Human Genetics 103, 431–439; September 6, 2018) Lisa Weixler has been added to the author list for her experimental and scientific contributions to the biophysical analysis of wild-type and mutant proteins. Her contributions were already mentioned in the acknowledgments. The authors apologize for initially only listing her in the acknowledgments and for the inconvenience. The author list has been corrected online and appears correctly here, and Lisa Weixler's affiliation is indicated as footnote 3: Center for Molecular Medicine Cologne, Cologne, Germany.

UR - http://www.scopus.com/inward/record.url?scp=85119899608&partnerID=8YFLogxK

U2 - 10.1016/j.ajhg.2021.11.013

DO - 10.1016/j.ajhg.2021.11.013

M3 - Comment/Letter to the editor

C2 - 34861176

AN - SCOPUS:85119899608

SN - 0002-9297

VL - 108

SP - 2385

JO - American journal of human genetics

JF - American journal of human genetics

IS - 12

ER -

Ghosh SG, Becker K, Huang H, Salazar TD, Chai G, Salpietro V et al. Erratum: Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome (The American Journal of Human Genetics (2018) 103(3) (431–439), (S0002929718302374), (10.1016/j.ajhg.2018.07.010)). American journal of human genetics. 2021 Dec 2;108(12):2385. doi: 10.1016/j.ajhg.2021.11.013

Erratum: Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome (The American Journal of Human Genetics (2018) 103(3) (431–439), (S0002929718302374), (10.1016/j.ajhg.2018.07.010))

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