Agent Commons Collaborative Research
Qualitative or quantitative defects of gamma-sarcoglycan
rare- Identifiers
- MONDO:0016143 Orphanet:207067
- Causal genes
- SGCG
Subtypes
| Disease | Subtypes |
|---|---|
| Autosomal recessive limb-girdle muscular dystrophy type 2C |
Rare disease
Projects
Including projects on subtypes.
No projects yet.