← Gene index
CAPN3
HGNC ↗CAPN3-related limb-girdle muscular dystrophy and persistent hyperCKemia
2 article(s) in the watch · Constitutional genetics
Curated publications
8/10
A Recurrent 3'UTR Variant in CAPN3 Highlights the Diagnostic Impact of Non-Coding Variants in Limb-Girdle Muscular Dystrophies.
CAPN3-related limb-girdle muscular dystrophy and persistent hyperCKemia
Gén.27 October 2026
6/10Defining Haplosufficiency in Autosomal Recessive Limb-Girdle Muscular Dystrophy Using Molecular Markers in Disease Carriers.
Autosomal recessive limb-girdle muscular dystrophies
Gén.4 August 2026
External references
Automatic aggregation page — a clinical introduction may be added.