Title : Molecular Pathogenesis of Familial Wolff-Parkinson-White Syndrome.

Pub. Date : 2018

PMID : 29593177






2 Functional Relationships(s)
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Protein Name
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1 Patients and animals with the mutation in PRKAG2 gene exhibit aberrant atrioventricular conduction associated with cardiac glycogen overload. Glycogen protein kinase AMP-activated non-catalytic subunit gamma 2 Homo sapiens
2 This review focuses on the molecular basis of the pathogenesis of cardiac abnormality due to PRKAG2 mutation and will provide current overviews of the mechanism of glycogen regulation by AMPK. Glycogen protein kinase AMP-activated non-catalytic subunit gamma 2 Homo sapiens