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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Bibliografiske detaljer
Udgivet i:Clin Cardiol
Main Authors: Li, Yuanhong, Wu, Gang, Tang, Qizhu, Huang, Congxin, Jiang, Hong, Shi, Lisong, Tu, Xin, Huang, Jinqi, Zhu, Xiaoqing, Wang, Hongli
Format: Artigo
Sprog:Inglês
Udgivet: Wiley Periodicals, Inc. 2010
Fag:
Clinical Investigations
Online adgang: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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