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Article

Random mitotic segregation of mitochondrial DNA in MELAS syndrome.

Acta neurologica Scandinavica - 1 Jan 2000

Huang C C, Chen R S, Chu N S, Pang C Y, Wei Y H

Abstract excerpt

We describe the heterogeneity of clinical features and molecular genetic characteristics of the probands and other members in two families with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS) syndrome. A point mutation at the 3243rd nucleotide position of mtDNA was found only in some of the maternal lineage members of the two families. Furthermore, the proportions of...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Identifiers

PMID: 8741143
DOI: 10.1111/j.1600-0404.1996.tb00199.x

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

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Random mitotic segregation of mitochondrial DNA in MELAS syndrome.PMID 8741143Read ↗

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