ATP Synthase Diseases of Mitochondrial Genetic Origin

Benzer Materyaller

• Molecular Basis of the Pathogenic Mechanism Induced by the m.9191T>C Mutation in Mitochondrial ATP6 Gene
  Yazar:: Su, Xin, ve diğerleri
  Baskı/Yayın Bilgisi: (2020)
• The pathogenic m.8993 T > G mutation in mitochondrial ATP6 gene prevents proton release from the subunit c-ring rotor of ATP synthase
  Yazar:: Su, Xin, ve diğerleri
  Baskı/Yayın Bilgisi: (2021)
• Identification of G8969>A in mitochondrial ATP6 gene that severely compromises ATP synthase function in a patient with IgA nephropathy
  Yazar:: Wen, Shuzhen, ve diğerleri
  Baskı/Yayın Bilgisi: (2016)
• Case Report: Identification of a Novel Variant (m.8909T>C) of Human Mitochondrial ATP6 Gene and Its Functional Consequences on Yeast ATP Synthase
  Yazar:: Ding, Qiuju, ve diğerleri
  Baskı/Yayın Bilgisi: (2020)
• Case Report: Identification of a Novel Variant (m.8909T>C) of Human Mitochondrial <i>ATP6</i> Gene and Its Functional Consequences on Yeast ATP Synthase
  Yazar:: Qiuju Ding, ve diğerleri
  Baskı/Yayın Bilgisi: (2020-09-01)