Nonsyndromic Parkinson disease in a family with autosomal dominant optic atrophy due to OPA1 mutations

Παρόμοια τεκμήρια

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