SDOCT Thickness Measurements of Various Retinal Layers in Patients with Autosomal Dominant Optic Atrophy due to OPA1 Mutations

Podobne zapisy

• OPA3 gene changes cause autosomal dominant optic atrophy
  Wydane: (2004)
• OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract
  od: Reynier, P, i wsp.
  Wydane: (2004)
• Optic disc morphology of patients with OPA1 autosomal dominant optic atrophy
  od: Votruba, M, i wsp.
  Wydane: (2003)
• Genomic deletions in OPA1 in Danish patients with autosomal dominant optic atrophy
  od: Almind, Gitte J, i wsp.
  Wydane: (2011)
• Subclinical multisystem neurologic disease in “pure” OPA1 autosomal dominant optic atrophy
  od: Baker, M.R., i wsp.
  Wydane: (2011)