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Article

Two novel mutations of the MYBPC3 gene identified in Chinese families with hypertrophic cardiomyopathy.

The Canadian journal of cardiology - 1 Dec 2010

Lin Jia, Zheng Dong-Dong, Tao Qin, Yang Jun-Hua, Jiang Wen-Ping, Yang Xiang-Jun, Song Jian-Ping, Jiang Ting-Bo, Li Xun

Abstract excerpt

BACKGROUND: Hypertrophic cardiomyopathy (HCM) is one of the most common genetic cardiovascular disorders. Mutations in the MYBPC3 gene are one of the most frequent genetic causes of HCM. OBJECTIVES: To screen MYBPC3 gene mutations in Chinese patients with HCM, and analyze the correlation between...

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Source

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Identifiers

PMID: 21165360
DOI: 10.1016/s0828-282x(10)70464-5
PMCID: PMC3006099

Genes

MYBPC3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-21165360-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

Related research

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Two novel mutations of the MYBPC3 gene identified in Chinese families with hypertrophic cardiomyopathy.PMID 21165360Read ↗

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A Novel Truncating Variant in MYBPC3 Causes Hypertrophic CardiomyopathySemantic proximity Read ↗

Familial hypertrophic cardiomyopathy: A case with a new mutation in the MYBPC3 gene.Semantic proximity Read ↗

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The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands.Semantic proximity Read ↗

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