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Summary Literature (0)
OMIM:601462 - MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL; CMS1A


Xenbase Genes: chrna1, chrna1.2, chrnd, chrne, chrnb1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011088 - congenital myasthenic syndrome 1A

Disease Ontology (DO):
DOID:0110663 - congenital myasthenic syndrome 1A