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Article

[Analysis of clinical phenotype in 42 nuclear pedigrees carrying mitochondrial DNA A3243G mutation].

Zhonghua yi xue za zhi - 7 Dec 2010

Ma Yi-nan, Fang Fang, Cao Yan-yan, Yang Yan-ling, Zou Li-ping, Zhang Ying, Wang Song-tao, Zhu Sai-nan, Li Lin, Zheng Xue-fei, Pei Pei, Wu Hai-rong, Xiao Yang, Qi Yu

Abstract excerpt

OBJECTIVE: A3243G mutation in mitochondrial DNA is the most common pathogenic point mutation causing a variety of phenotypes. The clinical phenotype and the relationship between the clinical phenotype and the ratio of A3243G mutation were studied in the members from nuclear families carrying A324...

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Identifiers

PMID: 21223764

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-21223764-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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