Nodoventricular accessory pathways in PRKAG2-dependent familial preexcitation syndrome reveal a disorder in cardiac development.

Circulation. Arrhythmia and electrophysiology

Volumn 1, Issue 4, 2008, Pages 276-281

  Tan, Hanno L ^a   van der Wal, Allard C ^a   Campian, Maria E ^a   Kruyswijk, Hittjo H ^a   ten Hove Jansen, Bram ^a   van Doorn, Dirk Jan ^a   Oskam, Henk J ^a   Becker, Anton E ^a   Wilde, Arthur A M ^a  

^a UNIVERSITY OF AMSTERDAM   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE KINASE; PRKAG2 PROTEIN, HUMAN;

ADULT; ARTICLE; COMPARATIVE STUDY; DISEASE COURSE; ELECTROCARDIOGRAPHY; ENZYMOLOGY; FEMALE; FOLLOW UP; GENETIC PREDISPOSITION; GENETICS; HEART LEFT VENTRICLE HYPERTROPHY; HEART MUSCLE; HEART PREEXCITATION; HUMAN; MALE; METABOLISM; MUTATION; NUCLEOTIDE SEQUENCE; PATHOLOGY; PATHOPHYSIOLOGY; PEDIGREE; PROGNOSIS; RETROSPECTIVE STUDY;

ADULT; AMP-ACTIVATED PROTEIN KINASES; DISEASE PROGRESSION; DNA; DNA MUTATIONAL ANALYSIS; ELECTROCARDIOGRAPHY; FEMALE; FOLLOW-UP STUDIES; GENETIC PREDISPOSITION TO DISEASE; HUMANS; HYPERTROPHY, LEFT VENTRICULAR; MALE; MUTATION; MYOCARDIUM; PEDIGREE; PRE-EXCITATION, MAHAIM-TYPE; PROGNOSIS; RETROSPECTIVE STUDIES;

EID: 70350496828     PISSN: None     EISSN: 19413084     Source Type: Journal    
DOI: 10.1161/CIRCEP.108.782862     Document Type: Article

References (0)