Condition: Wolff-Parkinson-White Syndrome


rs121908987 in PRKAG2 gene and Wolff-Parkinson-White Syndrome PMID 11407343 2001 Identification of a gene responsible for familial Wolff-Parkinson-White syndrome.

PMID 11748095 2001 Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy.

PMID 14722619 2004 CBS domains form energy-sensing modules whose binding of adenosine ligands is disrupted by disease mutations.