Variation in retinal nerve fiber layer thickness at different stages of Leber’s hereditary optic neuropathy in patients with the ND4 G11778A mutation
Author:
Affiliation:
1. Department of Ophthalmology, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei Province, China
Funder
National Natural Science Foundation of China
Horizontal Project Fund
Hubei Province Heath Oiffce on the project
Hubei Province Department of Education Guidance Project
Publisher
Informa UK Limited
Subject
Ophthalmology,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/08820538.2021.1986078
Reference16 articles.
1. Inherited mitochondrial optic neuropathies
2. Jia X, Li S, Xiao X, et al. Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy. J Hum Genet. 2006;51(10):851–856.
3. Adeno-associated virus-mediated gene delivery of the human ND4 complex I subunit in rabbit eyes
4. Applications of the method of high resolution melting analysis for diagnosis of Leber's disease and the three primary mutation spectrum of LHON in the Han Chinese population
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1. PhNR and peripapillary RNFL changes in Leber hereditary optic neuropathy with m.G11778A mutation;Mitochondrion;2023-05
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