Molecular Pathogenesis of Familial Wolff‐Parkinson‐White Syndrome: Molecular Mechanisms of Cardiac Glycogen Regulation by AMPK

Familial Wolff‐Parkinson‐White (WPW) syndrome is an autosomal dominant inherited disease and consists of a small percentage of WPW syndrome which exhibits ventricular pre‐excitation by development of accessory atrioventricular pathway. A series of mutations in PRKAG2 gene encoding gamma2 subunit of...

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Veröffentlicht in:	The Journal of Medical Investigation 2018, Vol.65(1.2), pp.1-8
1. Verfasser:	Miyamoto, Licht
Format:	Artikel
Sprache:	eng
Schlagworte:	5'AMP‐activated protein kinase aberrant atrioventricular conduction amilial Wolff‐Parkinson‐White Syndrome glycogen ventricular  pre‐excitation
Online-Zugang:	Volltext
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