Mitochondrial DNA Complex I and III Mutations Associated with Leber's Hereditary Optic Neuropathy

Ítems similars

• Pathological significance of the mtDNA COX III mutation at nucleotide pair 9438 in Leber hereditary optic neuropathy.
  per: Brown, M. D., et al.
  Publicat: (1994)
• Mitochondrial ND-I mutation in Leber hereditary optic neuropathy.
  per: Johns, D R
  Publicat: (1992)
• A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I.
  per: Brown, M D, et al.
  Publicat: (1992)
• Identification of novel mitochondrial mutations in Leber’s hereditary optic neuropathy
  per: Kumar, Manoj, et al.
  Publicat: (2010)
• Leber's hereditary optic neuropathy with 3460 mitochondrial DNA mutation.
  per: Hwang, Jeong-Min, et al.
  Publicat: (2002)