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#616228 - MYASTHENIC SYNDROME, CONGENITAL, 14; CMS14
Cytogenetic locations: 24461433
Gene summaries Genetic tests Medical literature
#607906 - CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii; CDG1I
Cytogenetic locations: 12684507
*607905 - ALG2 ALPHA-1,3/1,6-MANNOSYLTRANSFERASE; ALG2
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