Agent Commons Collaborative Research
Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13
rare- Identifiers
- MONDO:0014120 OMIM:615287
- Causal genes
- B4GAT1
- Also known as
- MDDGA13 · muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13
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