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Article

Heterogeneous tissue distribution of a mitochondrial DNA polymorphism in heteroplasmic subjects without mitochondrial disorders.

Journal of medical genetics - 1 May 2001

Kirches E, Michael M, Warich-Kirches M, Schneider T, Weis S, Krause G, Mawrin C, Dietzmann K

Abstract excerpt

CONTEXT: Several maternally inherited point mutations of the mitochondrial genome cause mitochondrial disorders, but the correlation between genotype and phenotype remains obscure in many cases. The same mutation may cause various diseases, probably because of a different tissue distribution. OBJECTIVE: To assess the role of random somatic segregation in generating interperson differences by analysis of an...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Polymorphism, Restriction Fragment Length

Share to Regulatory Sequences, Nucleic Acid

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Source

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Identifiers

PMID: 11333867
DOI: 10.1136/jmg.38.5.312
PMCID: PMC1734867

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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