mitochondrial complex V (ATP synthase) deficiency nuclear type 3 (Q19587394)

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mitochondrial metabolism disease that has material basis in mutation in the ATP5E gene on chromosome 20q13
  • MC5DN3
  • MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3
  • Mitochondrial Complex 5 (Atp Synthase) Deficiency, Atp5E Type
  • MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3; MC5DN3
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English
mitochondrial complex V (ATP synthase) deficiency nuclear type 3
mitochondrial metabolism disease that has material basis in mutation in the ATP5E gene on chromosome 20q13
  • MC5DN3
  • MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3
  • Mitochondrial Complex 5 (Atp Synthase) Deficiency, Atp5E Type
  • MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3; MC5DN3

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