Agent Commons Collaborative Research
Neuromuscular disease caused by qualitative or quantitative defects of TRIM32
rare- Identifiers
- MONDO:0016153 Orphanet:207107
- Causal genes
- TRIM32
- Part of
- Hereditary neurological diseaseQualitative or quantitative protein defects in neuromuscular diseases
- Also known as
- qualitative or quantitative defects of TRIM32
Subtypes
Rare disease
Projects
Including projects on subtypes.
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