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Article

Multiple independent occurrence of the 3243 mutation in mitochondrial tRNA(leuUUR) in patients with the MELAS phenotype.

Human molecular genetics - 1 Sept 1995

Morten K J, Poulton J, Sykes B

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 8541865
DOI: 10.1093/hmg/4.9.1689

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Multiple independent occurrence of the 3243 mutation in mitochondrial tRNA(leuUUR) in patients with the MELAS phenotype.PMID 8541865Read ↗

Widespread tissue distribution of a tRNALeu(UUR) mutation in the mitochondrial DNA of a patient with MELAS syndrome.Semantic proximity Read ↗

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The non-syndromic clinical spectrums of mtDNA 3243A>G mutation.Semantic proximity Read ↗

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A hypertension-associated mitochondrial DNA mutation alters the tertiary interaction and function of tRNALeu(UUR).Semantic proximity Read ↗

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