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Article

Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNA(Leu(UUR)) gene.

Muscle & nerve. Supplement - 1 Jan 1995

Koga Y, Davidson M, Schon E A, King M P

Abstract excerpt

MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes), a maternally inherited mitochondrial disorder, has been associated with an A-->G transition at nucleotide 3243 and a T-->C transition at nucleotide 3271, both in the mitochondrial tRNA(Leu(UUR)) gene. We transferred mitochondria harboring these mutations into human cells lacking endogenous mtDNA (rho o cells), and analyzed...

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Identifiers

PMID: 7603512
DOI: 10.1002/mus.880181424

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Analysis of cybrids harboring MELAS mutations in the mitochondrial tRNA(Leu(UUR)) gene.PMID 7603512Read ↗

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