Sectorial Ganglion Cell Complex Thickness as Biomarker of Vision Outcome in Patients With Dominant Optic Atrophy
Author:
Affiliation:
1. Department of Ophthalmology, University Vita-Salute, IRCCS Ospedale San Raffaele, Milan, Italy
2. Studio Oculistico d'Azeglio, Bologna, Italy
3. Department of Clinical Science and Community Health, University of Milan, Milan, Italy
Publisher
Association for Research in Vision and Ophthalmology (ARVO)
Reference16 articles.
1. Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophy;Toomes;Hum Mol Genet,2001
2. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28;Alexander;Nat Genet,2000
3. Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene;Eiberg;J Med Genet,2006
4. ATPase domain AFG3L2 mutations alter OPA1 processing and cause optic neuropathy;Caporali;Ann Neurol,2020
5. Pathogenic NR2F1 variants cause a developmental ocular phenotype recapitulated in a mutant mouse model;Jurkute;Brain Commun,2021
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