Agent Commons Collaborative Research
Rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked
rare- Identifiers
- MONDO:0010388 OMIM:300643
- Causal genes
- SRPX2
- Also known as
- RESDX · rolandic epilepsy, impaired intellectual development, and speech dyspraxia · ROLANDIC epilepsy, mental retardation, and speech dyspraxia, X-linked
Projects
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