Clinical, biochemical and molecular genetic features of Leber’s hereditary optic neuropathy
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Biochemistry,Biophysics
Reference118 articles.
Cited by 54 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. A splice-altering homozygous variant in COX18 causes severe sensory-motor neuropathy with oculofacial apraxia;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2024-10
2. Multi-mtDNA Variants May Be a Factor Contributing to Mitochondrial Function Variety in the Skin-Derived Fibroblasts of Leber's Hereditary Optic Neuropathy Patients;Frontiers in Molecular Neuroscience;2022-07-13
3. Clinical observations of Leber hereditary optic neuropathy with and without neurological symptoms;Annals of Clinical and Experimental Neurology;2022-01-15
4. Neuroprotection and Neurocognitive Augmentation by Photobiomodulation;Contemporary Clinical Neuroscience;2021
5. Optic neuropathy: A 15-year retrospective observational study;Multiple Sclerosis and Related Disorders;2020-09
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