Visual and psychological morbidity among patients with autosomal dominant optic atrophy

Gelijkaardige items

• OPA1 mutations impair mitochondrial function in both pure and complicated dominant optic atrophy
  door: Yu-Wai-Man, Patrick, et al.
  Gepubliceerd in: (2011)
• Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation
  door: Yu-Wai-Man, Patrick, et al.
  Gepubliceerd in: (2011)
• Subclinical multisystem neurologic disease in “pure” OPA1 autosomal dominant optic atrophy
  door: Baker, M.R., et al.
  Gepubliceerd in: (2011)
• Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of dominant optic atrophy
  door: Yu-Wai-Man, Patrick, et al.
  Gepubliceerd in: (2009)
• Dominant Optic Atrophy – Novel OPA1 Mutations and Revised Prevalence Estimates
  door: Yu-Wai-Man, Patrick, et al.
  Gepubliceerd in: (2013)