OPA1 mutations impair mitochondrial function in both pure and complicated dominant optic atrophy

Lignende værker

• Subclinical multisystem neurologic disease in “pure” OPA1 autosomal dominant optic atrophy
  af: Baker, M.R., et al.
  Udgivet: (2011)
• Dominant Optic Atrophy – Novel OPA1 Mutations and Revised Prevalence Estimates
  af: Yu-Wai-Man, Patrick, et al.
  Udgivet: (2013)
• Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation
  af: Yu-Wai-Man, Patrick, et al.
  Udgivet: (2011)
• Pattern of retinal ganglion cell loss in dominant optic atrophy due to OPA1 mutations
  af: Yu-Wai-Man, P, et al.
  Udgivet: (2011)
• The Prevalence and Natural History of Dominant Optic Atrophy due to OPA1 Mutations
  af: Yu-Wai-Man, Patrick, et al.
  Udgivet: (2010)