Calmodulinopathy in inherited arrhythmia syndromes

Calmodulinopathy in inherited arrhythmia syndromes

Calmodulin (CaM) is a ubiquitous intracellular calcium sensor that controls and regulates key cellular functions. In all vertebrates, three CaM genes located on separate chromosomes encode an identical 149 amino acid protein, implying an extraordinarily high level of evolutionary importance and sugg...

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Bibliographic Details
Main Authors: Wen-Chin Tsai, Peng-Sheng Chen, Michael Rubart
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2021-01-01
Series:Tzu-Chi Medical Journal
Subjects:
calmodulinopathy
catecholaminergic polymorphic ventricular tachycardia
long qt syndrome and inherited arrhythmia syndromes
Online Access:http://www.tcmjmed.com/article.asp?issn=1016-3190;year=2021;volume=33;issue=4;spage=339;epage=344;aulast=Tsai

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http://www.tcmjmed.com/article.asp?issn=1016-3190;year=2021;volume=33;issue=4;spage=339;epage=344;aulast=Tsai

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