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Summary Literature (0)
MIM:616321 - MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A

Xenbase Genes: chrnd

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014583 - congenital myasthenic syndrome 3A
MONDO:0018940 - congenital myasthenic syndrome
MONDO:0020344 - postsynaptic congenital myasthenic syndrome