No evidence of association between optic neuritis and secondary LHON mtDNA mutations in patients with multiple sclerosis
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Molecular Medicine
Reference33 articles.
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1. In silico model of mtDNA mutations effect on secondary and 3D structure of mitochondrial rRNA and tRNA in Leber’s hereditary optic neuropathy;Experimental Eye Research;2020-12
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3. Only pathogenic variants in protein-coding mtDNA genes cause Leigh syndrome;Journal of the Neurological Sciences;2019-12
4. Association of MS4A6A, CD33, and TREM2 gene polymorphisms with the late-onset Alzheimer’s disease;BioImpacts;2019-05-22
5. Mitochondrial DNA G15927A and G15928A variations in patients with multiple sclerosis;Multiple Sclerosis and Related Disorders;2019-01
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