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Article

[Relationship between electrocardiographic and genetic mutation (MYH7-H1717Q, MYLK2-K324E and KCNQ1-R190W) phenotype in patients with hypertrophic cardiomyopathy].

Zhonghua xin xue guan bing za zhi - 1 Jan 2016

Shao Hong, Zhang Yanmin, Liu Liwen, Ma Zhiling, Zuo Lei, Ye Chuang, Wei Xiaomei, Sun Chao, Tao Ling

Abstract excerpt

OBJECTIVE: To explore the relationship between electrocardiographic (ECG) and genetic mutations of patients with hypertrophic cardiomyopathy (HCM), and early ECG changes in HCM patients. METHODS: Clinical, 12-lead ECG and echocardiographic examination as well as genetic examinations were made in a three-generation Chinses HCM pedigree with 8 family members (4 males). The clinical characterization and ECG...

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Source

Identifiers

PMID: 26813553
DOI: 10.3760/cma.j.issn.0253-3758.2016.01.011

Genes

KCNQ1
MYLK2
MYH7
TMEM70

Variants

Provenance

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.

Related research

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[Relationship between electrocardiographic and genetic mutation (MYH7-H1717Q, MYLK2-K324E and KCNQ1-R190W) phenotype in patients with hypertrophic cardiomyopathy].PMID 26813553Read ↗

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