Carrying both the heterozygous Myh6-R453C and Tnnt2-R92W mutations aggravate the hypertrophic cardiomyopathy phenotype in mice-Reference-Cited by-同舟云学术

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Carrying both the heterozygous Myh6-R453C and Tnnt2-R92W mutations aggravate the hypertrophic cardiomyopathy phenotype in mice

Published:2024-11 Issue: Volume:733 Page:150582
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Lu Minjie^ORCID,Li Shuai,Han Ziqiang,Ma Bingxuan,Wang Leqi,Wan Fangfang,Lei Song,Nie Yu^ORCID,Wang Jizheng^ORCID

Funder

National Natural Science Foundation of China

Chinese Academy of Meteorological Sciences

China Academy of Chinese Medical Sciences

Publisher

Elsevier BV

Reference36 articles.

1. Diagnosis and evaluation of hypertrophic cardiomyopathy: JACC state-of-the-art review;Maron;J. Am. Coll. Cardiol.,2022

2. Clinical course and management of hypertrophic cardiomyopathy;Maron;N. Engl. J. Med.,2018

3. Penetrance of hypertrophic cardiomyopathy in sarcomere protein mutation carriers;Lorenzini;J. Am. Coll. Cardiol.,2020

4. Molecular genetic basis of hypertrophic cardiomyopathy;Marian;Circ. Res.,2021

5. The mammalian myosin heavy chain gene family;Weiss;Annu. Rev. Cell Dev. Biol.,1996

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