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#620358 - MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4A; MC5DN4A
Cytogenetic locations: 34954817
Gene summaries Genetic tests Medical literature
#616045 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 22; COXPD22
Cytogenetic locations: 23596069
#615228 - MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4B; MC5DN4B
*164360 - ATP SYNTHASE F1, SUBUNIT ALPHA; ATP5F1A
Cytogenetic locations: mutation
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