Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia

@PedsGIChat Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia. Am J Hum Genet. 2015 Dec 3;97(6):855-61. https://t.co/5xLs4mycTU

Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral… https://t.co/2sebus60un

PubMed: Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure,… https://t.co/p6YRkiEBjz

Mutaciones en el gen SCYL1 produce un síndrome con fallo hepático, neuropatía periférica, atrofia cerebelar y ataxia https://t.co/pLRXiNUcKQ