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GLUT1 Deficiency in a Patient Diagnosed as Cerebral Palsy: Is NGS a Valuable Tool to Be Considered in All Cases of CP to Detect Underlying Genetic Disorders?

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Bibliografiske detaljer
Udgivet i:Mov Disord Clin Pract
Main Authors: Méneret, Aurélie, Roze, Emmanuel
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley & Sons, Inc. 2019
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6476600/
https://ncbi.nlm.nih.gov/pubmed/31061833
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.12754
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