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#619012 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 48; COXPD48
Cytogenetic locations: 608501
Gene summaries Genetic tests Medical literature
*617491 - NOP2/SUN RNA METHYLTRANSFERASE FAMILY, MEMBER 3; NSUN3
*605345 - AlkB HOMOLOG 1, HISTONE H2A DIOXYGENASE; ALKBH1
Cytogenetic locations: 16482161
*590065 - TRANSFER RNA, MITOCHONDRIAL, METHIONINE; MTTM
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