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Article

MtDNA m.3472T>C could be classified as a primary mutation of Leber's hereditary optic neuropathy.

Journal of the neurological sciences - 15 Sept 2017

Seong Moon-Woo, Choi Jongmoon, Park Sung Sup, Kim Ji Yeon, Hwang Jeong-Min

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Share to DNA, Mitochondrial
Share to Mutation
Share to Optic Atrophy, Hereditary, Leber

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Identifiers

PMID: 28870561
DOI: 10.1016/j.jns.2017.07.017

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MtDNA m.3472T>C could be classified as a primary mutation of Leber's hereditary optic neuropathy.PMID 28870561Read ↗

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Mitochondrial DNA mutation m.3635G>A may be associated with Leber hereditary optic neuropathy in Chinese.Semantic proximity Read ↗

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Variable Presentation of Leber Hereditary Optic Neuropathy in Children of a Family Harboring a Rare m.13051G>A mtDNA Mutation.Semantic proximity Read ↗

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Mitochondrial tRNAThr 15891C>G mutation was not associated with Leber's hereditary optic neuropathy in Han Chinese patients.Semantic proximity Read ↗

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