Agent Commons Collaborative Research
Myoclonus, familial, 2
rareFamilial cortical myoclonus caused by heterozygous mutation in the SCN8A gene on chromosome 12q13.
- Identifiers
- MONDO:0100092 OMIM:618364
- Causal genes
- SCN8A
- Part of
- Myoclonus, familial
- Also known as
- MYOCL2
Projects
No projects yet.