Publication Name	World Journal of Clinical Cases
Manuscript ID	101272
Country	China

Received	2024-09-09 14:02
Peer-Review Started	2024-09-09 14:02
To Make the First Decision
Return for Revision	2024-10-22 13:10
Revised	2024-11-03 15:42
Second Decision	2025-01-06 02:40
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2025-01-07 09:56
Articles in Press	2025-01-07 09:56
Publication Fee Transferred	2024-11-14 12:55
Edit the Manuscript by Language Editor
Typeset the Manuscript	2025-01-15 08:10
Publish the Manuscript Online	2025-01-21 07:29

ISSN	2307-8960 (online)
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Category	Cardiac & Cardiovascular Systems
Manuscript Type	Case Report
Article Title	MYH7 mutation in a pedigree with familial dilated hypertrophic cardiomyopathy: A case report and review of literature
Manuscript Source	Unsolicited Manuscript
All Author List	Ying Hong, Zhen Fan, Yi Guo, Hui-Hui Ma, Sheng-Zhi Zeng, Hu-Tao Xi, Jing Yang, Kai Luo, Rong Luo and Xiao-Ping Li
ORCID	Author(s) ORCID Number Ying Hong http://orcid.org/0000-0003-4002-7868 Rong Luo http://orcid.org/0000-0003-3982-8772 Xiao-Ping Li http://orcid.org/0000-0001-5580-5605
Funding Agency and Grant Number	Funding Agency Grant Number National Natural Science Foundation of China 81770379
Corresponding Author	Xiao-Ping Li, PhD, Department of Cardiology, Sichuan Academy of Medical Sciences and Sichuan Provincial People’s Hospital, No. 32 Section 2 West 1st Ring Road, Chengdu 610072, Sichuan Province, China. lixiaoping0119@163.com
Key Words	Dilated phase of hypertrophic cardiomyopathy; Pedigree; MYH7 gene; Missense mutation; Literature review; Case report
Core Tip	A subset of patients with hypertrophic cardiomyopathy (HCM) progress to a dilated phase of HCM (DPHCM), which is associated with a poor prognosis. Our findings corroborate the pathogenicity of the MYH7 (c.746G>A, p.Arg249Glu) mutation for DPHCM, and we hypothesize that the Arg249Gln mutation in the MYH7 gene may be responsible for the high mortality of DPHCM.
Publish Date	2025-01-21 07:29
Citation	<p>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. <i>World J Clin Cases</i> 2025; 13(15): 101272</p>
URL	https://www.wjgnet.com/2307-8960/full/v13/i15/101272.htm
DOI	https://dx.doi.org/10.12998/wjcc.v13.i15.101272

Full Article (PDF)	WJCC-13-101272-with-cover.pdf
CARE Checklist–2016	101272-CARE-Checklist-2016.pdf
Manuscript File	101272_Auto_Edited_085159.docx
Answering Reviewers	101272-answering-reviewers.pdf
Audio Core Tip	101272-audio.m4a
Conflict-of-Interest Disclosure Form	101272-conflict-of-interest-statement.pdf
Copyright License Agreement	101272-copyright-assignment.pdf
Approved Grant Application Form(s) or Funding Agency Copy of any Approval Document(s)	101272-foundation-statement.pdf
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Non-Native Speakers of English Editing Certificate	101272-non-native-speakers.pdf
Peer-review Report	101272-peer-reviews.pdf
Scientific Misconduct Check	101272-scientific-misconduct-check.png
Scientific Editor Work List	101272-scientific-editor-work-list.pdf
CrossCheck Report	101272-crosscheck-report.pdf