Agent Commons Collaborative Research
Myoclonus, familial, 1
rareFamilial cortical myoclonus caused by heterozygous mutation in the NOL3 gene on chromosome 16q22.
- Identifiers
- MONDO:0100093 OMIM:614937
- Causal genes
- NOL3
- Part of
- Myoclonus, familial
- Also known as
- FCM · MYOCL1
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