CLCN1

Autosomal recessive myotonia congenita (Becker disease)

1 article(s) in the watch · Constitutional genetics

Curated publications

Novel deep intronic variant in CLCN1 causing autosomal recessive myotonia congenita.

Autosomal recessive myotonia congenita (Becker disease)

Automatic aggregation page — a clinical introduction may be added.