Mutation Screening of Mitochondrial DNA as Well as OPA1 and OPA3 in a Chinese Cohort With Suspected Hereditary Optic Atrophy-Reference-Cited by-同舟云学术

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Mutation Screening of Mitochondrial DNA as Well as OPA1 and OPA3 in a Chinese Cohort With Suspected Hereditary Optic Atrophy

Published:2014-09-09 Issue:10 Volume:55 Page:6987-6995
ISSN:0146-0404
Container-title:Investigative Ophthalmology & Visual Science
language:en
Short-container-title:Investigative Ophthalmology & Visual Science

Author:

Chen J.,Xu K.,Zhang X.,Jiang F.,Liu L.,Dong B.,Ren Y.,Li Y.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Cited by 24 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. Severe mitochondrial encephalomyopathy caused by de novo variants in OPA1 gene;Frontiers in Genetics;2024-08-20

2. Mitochondrial dynamics and mitochondrial autophagy: Molecular structure, orchestrating mechanism and related disorders;Mitochondrion;2024-03

3. Oxidative Stress in Antibiotic Toxic Optic Neuropathy Mimicking Acute LHON in a Patient with Exacerbation of Cystic Fibrosis;Stresses;2023-03-14

4. OPA1 Dominant Optic Atrophy: Diagnostic Approach in the Pediatric Population;Current Issues in Molecular Biology;2023-01-05

5. Comprehensive Genetic Analysis Unraveled the Missing Heritability in a Chinese Cohort With Wolfram Syndrome 1: Clinical and Genetic Findings;Investigative Opthalmology & Visual Science;2022-09-13

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