MYH7 mutation in a pedigree with familial dilated hypertrophic cardiomyopathy: A case report and review of literature

doi:10.12998/wjcc.v13.i15.101272

Advanced Search

BPG is committed to discovery and dissemination of knowledge

Home / Archive / Volume 13, Issue 15

This Article

Academic Content and Language Evaluation of This Article

CrossCheck and Google Search of This Article

Academic Rules and Norms of This Article

Citation of this article

Corresponding Author of This Article

Research Domain of This Article

Article-Type of This Article

Open-Access Policy of This Article

Times Cited Counts in Google of This Article

Number of Hits and Downloads for This Article

Total Article Views (596)

All Articles published online

The chart showing PDF series, HTML series, Figures (1-5) series, Tables (1-2) series.

Item

Count

PDF

HTML

278

Figures (1-5)

114

Tables (1-2)

Sum=508

Publishing Process of This Article

The chart showing Browse series, Download series.

Item

Count

Browse

Download

Sum=56

May 26, 2025 (publication date) through Mar 7, 2025

Times Cited of This Article

Times Cited (0)

Journal Information of This Article

Publication Name

World Journal of Clinical Cases

ISSN

2307-8960

Publisher of This Article

Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

Case Report

World J Clin Cases. May 26, 2025; 13(15): 101272
Published online May 26, 2025. doi: 10.12998/wjcc.v13.i15.101272

Full Size Figure Download Figure

Figure 2 The electrocardiogram of the proband showed sinus rhythm and the S-T segment of leads I, avL and V6 was depressed and the T wave was inverted change.

Citation: Hong Y, Fan Z, Guo Y, Ma HH, Zeng SZ, Xi HT, Yang J, Luo K, Luo R, Li XP. MYH7 mutation in a pedigree with familial dilated hypertrophic cardiomyopathy: A case report and review of literature. World J Clin Cases 2025; 13(15): 101272
URL: https://www.wjgnet.com/2307-8960/full/v13/i15/101272.htm
DOI: https://dx.doi.org/10.12998/wjcc.v13.i15.101272