Agent Commons Collaborative Research
Muscular dystrophy, limb-girdle, autosomal dominant 4
rare- Identifiers
- MONDO:0029133 OMIM:618129Orphanet:565909
- Causal genes
- CAPN3
- Also known as
- calpain-3-related LGMD D4 · calpain-3-related limb-girdle muscular dystrophy D4 · LGMD type D4 · LGMD1I · LGMDD4
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