Title : Confirmation of mutations in PROSC as a novel cause of vitamin B 6 -dependent epilepsy.

Pub. Date : 2017 Dec

PMID : 28391250






1 Functional Relationships(s)
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1 Vitamin-B6-dependent epilepsies are a heterogenous group of treatable disorders due to mutations in several genes (ALDH7A1, PNPO, ALPL or ALDH4A1). Vitamin B 6 aldehyde dehydrogenase 7 family member A1 Homo sapiens