A recurrent deletion mutation in OPA1 causes autosomal dominant optic atrophy in a Chinese family | Scientific Reports
A Missense Mutation in OPA1 Causes Dominant Optic Atrophy in a Chinese Family
An 18-year-old man with dominant optic atrophy (DOA). The fundus... | Download Scientific Diagram
Autosomal dominant optic atrophy - American Academy of Ophthalmology
Leber's Hereditary Optic Neuropathy – Case-Based Neuro-Ophthalmology
Dominant optic atrophy | Orphanet Journal of Rare Diseases | Full Text
Frontiers | The Role of Mitochondria in Optic Atrophy With Autosomal Inheritance
Comparison of the clinical and genetic features of autosomal dominant optic atrophy and normal tension glaucoma in young Chinese adults | Eye
Typical fundal appearance in dominant optic atrophy showing bilateral... | Download Scientific Diagram
Autosomal Dominant Optic Atrophy Plus Syndrome: A Case Report
EyeRounds.org:Dominant Optic Atrophy: 47 year-old female with chronic, mildly subnormal vision
Atlas Entry - Dominant optic atrophy
Autosomal Dominant Optic Atrophy - is a condition that mainly affects vision, but may include other features. | Dominant, Nurse practitioner, Conditioner
Autosomal dominant optic atrophy and cataract: MedlinePlus Genetics
New gene therapy could treat dominant optic atrophy
First submicroscopic inversion of the OPA1 gene identified in dominant optic atrophy – a case report | BMC Medical Genetics | Full Text
ADOA - Stoke Therapeutics
Atlas Entry - Dominant optic atrophy
Delayed diagnosis of autosomal dominant optic atrophy until seventh decade of life - Canadian Journal of Ophthalmology
AUTSOMAL DOMINANT OPTIC ATROPHY (ADOA) – Rome Vision Clinic di Andrea Cusumano
Autosomal Dominant Optic Atrophy - an overview | ScienceDirect Topics
Optic Atrophy - EyeWiki
