Slow Cardiac Myosin Regulatory Light Chain 2 (MYL2) was Down‐Expressed in Chronic Heart Failure Patients

BACKGROUND: Genetic studies have shown that many slow cardiac myosin regulatory light chain 2 (MYL2) gene mutations can cause hypertrophic cardiomyopathy, which is one of the most common causes of heart failure (HF). But until now there has been no pathological or histological evidence that MYL2 may...

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Detalhes bibliográficos
Publicado no:Clin Cardiol
Main Authors: Li, Yuanhong, Wu, Gang, Tang, Qizhu, Huang, Congxin, Jiang, Hong, Shi, Lisong, Tu, Xin, Huang, Jinqi, Zhu, Xiaoqing, Wang, Hongli
Formato: Artigo
Idioma:Inglês
Publicado em: Wiley Periodicals, Inc. 2010
Assuntos:
Clinical Investigations
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6652384/
https://ncbi.nlm.nih.gov/pubmed/21259275
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/clc.20832
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