Leber's Hereditary Optic Neuropathy: The Etiological Role of a Mutation in the Mitochondrial Cytochrome B Gene

Samankaltaisia teoksia

• Phylogenetic Analysis of the Mitochondrial Genomes from Leber Hereditary Optic Neuropathy Pedigrees
  Tekijä: Howell, N., et al.
  Julkaistu: (1995)
• A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology.
  Tekijä: Mackey, D, et al.
  Julkaistu: (1992)
• Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.
  Tekijä: Howell, N, et al.
  Julkaistu: (1991)
• Mitochondrial ND-I mutation in Leber hereditary optic neuropathy.
  Tekijä: Johns, D R
  Julkaistu: (1992)
• When does bilateral optic atrophy become Leber hereditary optic neuropathy?
  Tekijä: Howell, N, et al.
  Julkaistu: (1993)