POR

P450 oxidoreductase deficiency (PORD — MIM#613571) — severe form

1 article(s) in the watch · Constitutional genetics

Curated publications

A Novel POR G88S Mutation Causes Severe PORD and Establishes a Critical Pharmacogenomic Risk Profile

P450 oxidoreductase deficiency (PORD — MIM#613571) — severe form

Automatic aggregation page — a clinical introduction may be added.