Medicina Genómica,
Mutaciones en el gen SCYL1 dan lugar a un síndrome con fallo hepático, neuropatía periférica, atrofia cerebelar y ataxia
Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia
Overview of attention for article published in American Journal of Human Genetics, November 2015
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