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#616323 - MYASTHENIC SYNDROME, CONGENITAL, 3C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS3C
Cytogenetic locations: 16916845
Gene summaries Genetic tests Medical literature
#616322 - MYASTHENIC SYNDROME, CONGENITAL, 3B, FAST-CHANNEL; CMS3B
Cytogenetic locations: 14592870
#616321 - MYASTHENIC SYNDROME, CONGENITAL, 3A, SLOW-CHANNEL; CMS3A
#253290 - MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE; LMPS
Cytogenetic locations: 1p36, 1p36, 1p36
*100720 - CHOLINERGIC RECEPTOR, NICOTINIC, DELTA POLYPEPTIDE; CHRND
Cytogenetic locations: 12499478
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