Identification of an ND4 Mutation in Leber Hereditary Optic Neuropathy
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Optometry,Ophthalmology
Reference36 articles.
1. Two Families with Leber's Hereditary Optic Neuropathy Carrying G11778A and T14502C Mutations with Haplogroup H2a2a1 in Mitochondrial DNA;Mol Med Rep,2015
2. Pathogenic Mitochondrial DNA Mutations and Associated Clinical Features in Korean Patients with Leber's Hereditary Optic Neuropathy;Invest Ophthalmol Vis Sci,2014
3. m.3635G>A Mutation as a Cause of Leber Hereditary Optic Neuropathy;J Clin Pathol,2014
4. Leber's Hereditary Optic Neuropathy-gene Therapy: From Benchtop to Bedside;J Ophthalmol,2011
5. Leber Hereditary Optic Neuropathy—Historical Report in Comparison with the Current Knowledge;Gene,2015
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1. An SCN1A gene missense variant in a Chinese Tujia ethnic family with genetic epilepsy with febrile seizures plus;Frontiers in Neurology;2023-07-27
2. Leber’s Hereditary Optic Neuropathy with Mitochondrial DNA Mutation G11778A: A Systematic Literature Review and Meta-Analysis;BioMed Research International;2023-01-24
3. Clinical profile of patients with leber hereditary optic neuropathy (LHON): An ambispective study of North Indian Cohorts;Annals of Indian Academy of Neurology;2022
4. Current and Emerging Treatment Modalities for Leber’s Hereditary Optic Neuropathy: A Review of the Literature;Advances in Therapy;2018-09-01
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