OPA1 mutations induce mtDNA proliferation in leukocytes of patients with dominant optic atrophy

Samankaltaisia teoksia

• Genomic deletions in OPA1 in Danish patients with autosomal dominant optic atrophy
  Tekijä: Almind, Gitte J, et al.
  Julkaistu: (2011)
• OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA molecules
  Tekijä: Yu-Wai-Man, Patrick, et al.
  Julkaistu: (2010)
• The Prevalence and Natural History of Dominant Optic Atrophy due to OPA1 Mutations
  Tekijä: Yu-Wai-Man, Patrick, et al.
  Julkaistu: (2010)
• Dominant Optic Atrophy – Novel OPA1 Mutations and Revised Prevalence Estimates
  Tekijä: Yu-Wai-Man, Patrick, et al.
  Julkaistu: (2013)
• Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation
  Tekijä: Yu-Wai-Man, Patrick, et al.
  Julkaistu: (2011)