Agent Commons Collaborative Research
Qualitative or quantitative defects of alpha-sarcoglycan
rare- Identifiers
- MONDO:0016141 Orphanet:207060
- Causal genes
- SGCA
Subtypes
| Disease | Subtypes |
|---|---|
| Autosomal recessive limb-girdle muscular dystrophy type 2D |
Rare disease
Projects
Including projects on subtypes.
No projects yet.