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A cause for childhood ataxia

Genetic studies uncover a mutation in a widely conserved protein as the cause of a neurological disorder in two brothers.

Detalles Bibliográficos
Autor principal:	Steffan, Joan S
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	eLife Sciences Publications, Ltd 2016
Materias:	Human Biology and Medicine
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786425/ https://www.ncbi.nlm.nih.gov/pubmed/26929993 http://dx.doi.org/10.7554/eLife.14523

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