SLC12A5

KCC2-developmental and epileptic encephalopathy (KCC2-DEE) — severe neonatal EIMFS

1 article(s) in the watch · Constitutional genetics

Curated publications

Compound heterozygous SLC12A5 variants expand the molecular and functional spectrum of KCC2-developmental and epileptic encephalopathy

KCC2-developmental and epileptic encephalopathy (KCC2-DEE) — severe neonatal EIMFS

Automatic aggregation page — a clinical introduction may be added.