Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms

D. Cheillan, M.J. Curt, G. Briand, G.S. Salomons, K. Mention-Mulliez, D. Dobbelaere, J.M. Cuisset, L. Lion-Francois, V.D. Portes, A. Chabli, V. Valayannopoulos, J.F. Benoist, J.M. Pinard, G. Simard, O. Douay, K. Deiva, A. Afenjar, D. Heron, F. Rivier, B. ChabrolF. Prieur, F. Cartault, G. Pitelet, A. Goldenberg, S. Bekri, M. Gerard, R. Delorme, M. Tardieu, N. Porchet, C. Vianey-Saban, J. Vamecq

Research output: Contribution to journalArticleAcademicpeer-review

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Original languageUndefined/Unknown
Article number96
JournalOrphanet Journal of Rare Diseases
Volume7
DOIs
Publication statusPublished - 2012

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