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Summary Literature (0)
MIM:614198 - MYASTHENIC SYNDROME, CONGENITAL, 16; CMS16

Xenbase Genes: scn4a

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013620 - congenital myasthenic syndrome 16
MONDO:0018940 - congenital myasthenic syndrome
MONDO:0020344 - postsynaptic congenital myasthenic syndrome