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#610542 - MYASTHENIC SYNDROME, CONGENITAL, 12; CMS12
Cytogenetic locations: 16870884
Gene summaries Genetic tests Medical literature
#608931 - MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY; CMS4C
Cytogenetic locations: 11030414
*138292 - GLUTAMINE:FRUCTOSE-6-PHOSPHATE AMIDOTRANSFERASE 1; GFPT1
GFPT1L, INCLUDED
Cytogenetic locations: 27607664
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