|
MIM:608931 - MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS4C
Echinobase Genes:
Human Disease Resource: OMIM
DOID:0110679 - congenital myasthenic syndrome 4C |
|
DOID:0110679 - congenital myasthenic syndrome 4C |