OPA1 Dominant Optic Atrophy: Pathogenesis and Therapeutic Targets-Reference-Cited by-同舟云学术

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OPA1 Dominant Optic Atrophy: Pathogenesis and Therapeutic Targets

Published:2023-04-19 Issue:4 Volume:43 Page:464-474
ISSN:1070-8022
Container-title:Journal of Neuro-Ophthalmology
language:en
Short-container-title:

Author:

Wong David C. S.^ORCID,Harvey Joshua P.,Jurkute Neringa,Thomasy Sara M.,Moosajee Mariya,Yu-Wai-Man Patrick,Gilhooley Michael J.^ORCID

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical),Ophthalmology

Reference116 articles.

1. Hereditary optic neuropathies;Newman;Eye,2004

2. A frameshift mutation in exon 28 of the OPA1 gene explains the high prevalence of dominant optic atrophy in the Danish population: evidence for a founder effect;Thiselton;Hum Genet.,2001

3. Dominant optic atrophy: novel OPA1 mutations and revised prevalence estimates;Yu-Wai-Man;Ophthalmology,2013

4. Quality of life in patients with leber hereditary optic neuropathy;Kirkman;Invest Ophthalmol Vis Sci.,2009

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hereditary Optic Neuropathies: An Updated Review;Journal of Clinical & Translational Ophthalmology;2024-06-26

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