T14484C and T14502C in the mitochondrial ND6 gene are associated with Leber’s hereditary optic neuropathy in a Chinese family
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Molecular Medicine
Reference31 articles.
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3. Phylogenetic analysis of Leber’s hereditary optic neuropathy mitochondrial DNA’s indicates multiple independent occurrences of the common mutations;Brown;Hum. Mutat.,1995
4. Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber’s hereditary optic neuropathy mtDNA mutations;Brown;J. Biol. Chem.,2000
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2. Maternally inherited non-syndromic hearing loss is linked with a novel mitochondrial ND6 gene mutation;Irish Journal of Medical Science (1971 -);2023-08-10
3. Clinically Diagnosed Occult Macular Dystrophy Habouring an m.14502T>C Mitochondrial DNA Mutation Associated with Leber’s Hereditary Optic Neuropathy: Case Report and Literature Review;Neuro-Ophthalmology;2023-07-05
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5. Mutational analysis of mitochondrial tRNA genes in 138 patients with Leber’s hereditary optic neuropathy;Irish Journal of Medical Science (1971 -);2021-05-29
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