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#614750 - MYASTHENIC SYNDROME, CONGENITAL, 13; CMS13
Cytogenetic locations: 16870884
Gene summaries Genetic tests Medical literature
#608093 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ij; CDG1J
Cytogenetic locations: 22304930
*191350 - DOLICHYL-PHOSPHATE N-ACETYLGLUCOSAMINE PHOSPHOTRANSFERASE; DPAGT1
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