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Article

[Comparative study of gene mutation between Chinese patients with familial and sporadic hypertrophic cardiomyopathy].

Zhonghua yi xue za zhi - 14 Nov 2006

Pan Guo-zhong, Liu Wen-ling, Hu Da-yi, Xie Wen-li, Zhu Tian-gang, Li Lei, Li Cui-lan, Bian Hong

Abstract excerpt

OBJECTIVE: To compare the gene mutation between Chinese patients with familial and sporadic hypertrophic cardiomyopathy (HCM). METHODS: Peripheral blood samples were collected from 36 patients with familial HCM (FHCM) and 50 patients with sporadic HCM (SHCM), all un-related and from different provinces of China. PCR was used to amplify the 26 protein-coding axons of beta-myosin heavy chain (MYH7), 16 exons for...

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Source

Identifiers

PMID: 17288815

Genes

MYH7
MYBPC3
TNNT2

Provenance

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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