Severe hypertrophic cardiomyopathy in a patient with a homozygous MYH7 gene variant-Reference-Cited by-同舟云学术

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Severe hypertrophic cardiomyopathy in a patient with a homozygous MYH7 gene variant

Published:2022-12 Issue:12 Volume:8 Page:e12373
ISSN:2405-8440
Container-title:Heliyon
language:en
Short-container-title:Heliyon

Author:

Serra Walter^ORCID,Vitetta Giulia,Uliana Vera,Barocelli Federico^ORCID,Barili Valeria^ORCID,Allegri Isabella,Ardissino Diego,Gualandi Francesca,Percesepe Antonio^ORCID

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference14 articles.

1. 2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the task force for the diagnosis and management of hypertrophic cardiomyopathy of the European Society of Cardiology (ESC);Elliott;Eur. Heart J.,2014

2. Genetic basis of hypertrophic cardiomyopathy;Lind;Expert Rev. Cardiovasc Ther.,2006

3. Hypertrophic cardiomyopathy: from gene defect to clinical disease;Chung;Cell Res.,2003

4. Familial hypertrophic cardiomyopathy: genes, mutations and animal models. A review;Ramírez;Invest. Clin.,2004

5. Mutations in MYBPC3 and MYH7 in association with brugada type 1 ECG pattern: overlap between brugada syndrome and hypertrophic cardiomyopathy?;Alessandra;Cardiogenetics,2021

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. HSPD1 is a biomarker related to poor prognosis and tumor immune microenvironment in Head and Neck Squamous Cell Carcinoma by Bioinformatics and Cancer Database Analysis;2024-07-29

2. Hypertrophic Cardiomyopathy: Genetic Foundations, Outcomes, Interconnections, and Their Modifiers;Medicina;2023-08-04

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