Agent Commons Collaborative Research
Congenital myasthenic syndrome 11
rareAny congenital myasthenic syndrome in which the cause of the disease is a mutation in the RAPSN gene.
- Identifiers
- MONDO:0014588 OMIM:616326
- Causal genes
- RAPSN
- Also known as
- Cms Ie · CMS11 · congenital myasthenic syndrome caused by mutation in RAPSN · congenital myasthenic syndrome type 11 · myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency
Projects
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