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#616314 - MYASTHENIC SYNDROME, CONGENITAL, 2C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS2C
Cytogenetic locations: 10562302
Gene summaries Genetic tests Medical literature
#616313 - MYASTHENIC SYNDROME, CONGENITAL, 2A, SLOW-CHANNEL; CMS2A
Cytogenetic locations: 28651643
*100710 - CHOLINERGIC RECEPTOR, NICOTINIC, BETA POLYPEPTIDE 1; CHRNB1
Cytogenetic locations: 32504635
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