Associated Papers
SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN).
Lenz D et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2018
Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia.
Schmidt WM et al.
American Journal of Human Genetics, 2015
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