Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

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...

Topics

Adolescent
Adult
Asian People
Base Sequence
Cardiomyopathy, Hypertrophic
Cardiomyopathy, Hypertrophic, Familial
Carrier Proteins
Child
Child, Preschool
China
DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Female

Genotype

Humans

Infant

Male

Middle Aged

Mutation

Source

Identifiers

PMID: 17288815

Genes

MYH7
MYBPC3
TNNT2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Comparative study of gene mutation between Chinese patients with familial and sporadic hypertrophic cardiomyopathy].PMID 17288815Read ↗

[Analysis of MYH7, MYBPC3 and TNNT2 gene mutations in 10 Chinese pedigrees with familial hypertrophic cardiomyopathy and the correlation between genotype and phenotype].Semantic proximity Read ↗

[Mutation and clinical relevance in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy].Semantic proximity Read ↗

[Analysis of phenotype and MYH7 gene variant in a family of patients with hypertrophic cardiomyopathy].Semantic proximity Read ↗

[The genotype-phenotype correlation of the MYH7 gene c.1273G > a mutation in familial hypertrophic cardiomyopathy].Semantic proximity Read ↗

[Genetic heterogeneity of myosin heavy chain 7 gene G823E mutation in familial hypertrophic cardiomyopathy in Chinese].Semantic proximity Read ↗

[Mutation analysis of beta myosin heavy chain gene in hypertrophic cardiomyopathy families].Semantic proximity Read ↗

[Screening and analysis of the mutations on beta-myosin heavy chain gene in 3 Chinese families with hypertrophic cardiomyopathy].Semantic proximity Read ↗

Mutations profile in Chinese patients with hypertrophic cardiomyopathy.Semantic proximity Read ↗

[Pro731Ser mutation in the β-myosin heavy chain and hypertrophic cardiomyopathy in a Chinese pedigree].Semantic proximity Read ↗

[Novel mutations of cardiac troponin T in Chinese patients with hypertrophic cardiomyopathy].Semantic proximity Read ↗

Prevalence and Distribution of Sarcomeric Gene Mutations in Japanese Patients With Familial Hypertrophic CardiomyopathySemantic proximity Read ↗

Screening of MYH7 gene mutation sites in hypertrophic cardiomyopathy and its significance.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.