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Year | Number of Results |
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1978 | 1 |
2009 | 1 |
2022 | 1 |
2024 | 0 |
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Vitamin B12 in Leber hereditary optic neuropathy mutation carriers: a prospective cohort study.
Orphanet J Rare Dis. 2022 Aug 9;17(1):310. doi: 10.1186/s13023-022-02453-z.
Orphanet J Rare Dis. 2022.
PMID: 35945620
Free PMC article.
Mitochondrial mutant cells are hypersensitive to ionizing radiation, phleomycin and mitomycin C.
Kulkarni R, Reither A, Thomas RA, Tucker JD.
Kulkarni R, et al.
Mutat Res. 2009 Apr 26;663(1-2):46-51. doi: 10.1016/j.mrfmmm.2009.01.004. Epub 2009 Feb 4.
Mutat Res. 2009.
PMID: 19428369
Single nucleotide mutations in mitochondrial genes involved in ATP synthesis result in a broad range of diseases. Leber optic atrophy and Leigh's syndrome are two such diseases arising from point mutations in the mitochondrial genome. ...
Single nucleotide mutations in mitochondrial genes involved in ATP synthesis result in a broad range of diseases. Leber optic …
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Charcot-Marie-Tooth disease with Leber optic atrophy.
McLeod JG, Low PA, Morgan JA.
McLeod JG, et al.
Neurology. 1978 Feb;28(2):179-84. doi: 10.1212/wnl.28.2.179.
Neurology. 1978.
PMID: 563998
The clinical features and mode of inheritance of the visual failure were those of Leber optic atrophy. The two conditions were inherited independently....
The clinical features and mode of inheritance of the visual failure were those of Leber optic atrophy. The two conditio …
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