Pathological significance of the mtDNA COX III mutation at nucleotide pair 9438 in Leber hereditary optic neuropathy.

Ítems similars

• Simultaneous occurrence of the 11778 (ND4) and the 9438 (COX III) mtDNA mutations in Leber hereditary optic neuropathy: molecular, biochemical, and clinical findings.
  per: Oostra, R J, et al.
  Publicat: (1995)
• MtDNA and Leber’s hereditary optic neuropathy
  per: Ding, Yu, et al.
  Publicat: (2017)
• Mouse mtDNA mutant model of Leber hereditary optic neuropathy
  per: Lin, Chun Shi, et al.
  Publicat: (2012)
• Mitochondrial DNA Complex I and III Mutations Associated with Leber's Hereditary Optic Neuropathy
  per: Brown, M. D., et al.
  Publicat: (1992)
• Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.
  per: Brown, M D, et al.
  Publicat: (1997)