(Q19587395)
English
mitochondrial complex V (ATP synthase) deficiency nuclear type 4
mitochondrial metabolism disease that has material basis in mutation in the ATP5A1 gene on chromosome 18q
- MC5DN4
- Mitochondrial Complex 5 (Atp Synthase) Deficiency, Atp5A1 Type
- MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4; MC5DN4
- MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4
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