SNX14

SCAR20 (autosomal recessive spinocerebellar ataxia type 20)

1 article(s) in the watch · Constitutional genetics

Curated publications

A Homozygous Deep Intronic SNX14 Variant Activates Pseudo-Exon Inclusion in a Patient with SCAR20

SCAR20 (autosomal recessive spinocerebellar ataxia type 20)

Automatic aggregation page — a clinical introduction may be added.