Subclinical multisystem neurologic disease in “pure” OPA1 autosomal dominant optic atrophy

समान संसाधन

• OPA1 mutations impair mitochondrial function in both pure and complicated dominant optic atrophy
  द्वारा: Yu-Wai-Man, Patrick, और अन्य
  प्रकाशित: (2011)
• Pattern of retinal ganglion cell loss in dominant optic atrophy due to OPA1 mutations
  द्वारा: Yu-Wai-Man, P, और अन्य
  प्रकाशित: (2011)
• OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract
  द्वारा: Reynier, P, और अन्य
  प्रकाशित: (2004)
• Visual and psychological morbidity among patients with autosomal dominant optic atrophy
  द्वारा: Bailie, Maura, और अन्य
  प्रकाशित: (2013)
• Dominant Optic Atrophy – Novel OPA1 Mutations and Revised Prevalence Estimates
  द्वारा: Yu-Wai-Man, Patrick, और अन्य
  प्रकाशित: (2013)