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Article

Mutations of the mitochondrial ND1 gene as a cause of MELAS.

Journal of medical genetics - 1 Oct 2004

Kirby D M, McFarland R, Ohtake A, Dunning C, Ryan M T, Wilson C, Ketteridge D, Turnbull D M, Thorburn D R, Taylor R W

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Share to Cells, Cultured
Share to DNA, Mitochondrial
Share to Electron Transport Complex I
Share to Fibroblasts

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to MELAS Syndrome

Share to Mitochondria

Share to Muscle, Skeletal

Share to NADH Dehydrogenase

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Identifiers

PMID: 15466014
DOI: 10.1136/jmg.2004.020537
PMCID: PMC1735602

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Related research

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Mutations of the mitochondrial ND1 gene as a cause of MELAS.PMID 15466014Read ↗

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The role of complex I genes in MELAS: a novel heteroplasmic mutation 3380G>A in ND1 of mtDNA.Semantic proximity Read ↗

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