Novel PRKAG2 Mutation Responsible for the Genetic Syndrome of Ventricular Preexcitation and Conduction System Disease With Childhood Onset and Absence of Cardiac Hypertrophy | Zendy

Michael H. Gollob | Zendy; John J. Seger | Zendy; Tanya N. Gollob | Zendy; Terry Tapscott | Zendy; Oscar Gonzales | Zendy; Linda L. Bachinski | Zendy; Robert J. Roberts | Zendy

Open Access

Novel PRKAG2 Mutation Responsible for the Genetic Syndrome of Ventricular Preexcitation and Conduction System Disease With Childhood Onset and Absence of Cardiac Hypertrophy

Author(s) -

Michael H. Gollob,

John J. Seger,

Tanya N. Gollob,

Terry Tapscott,

Oscar Gonzales,

Linda L. Bachinski,

Robert J. Roberts

Publication year - 2001

Publication title -

circulation

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 7.795

H-Index - 607

eISSN - 1524-4539

pISSN - 0009-7322

DOI - 10.1161/hc5001.102111

Subject(s) - medicine , missense mutation , cardiology , atrial fibrillation , mutation , left ventricular hypertrophy , genetics , gene , biology , blood pressure

We recently reported a mutation in the PRKAG2 gene to be responsible for a familial syndrome of ventricular preexcitation, atrial fibrillation, conduction defects, and cardiac hypertrophy. We now report a novel mutation in PRKAG2 causing Wolff-Parkinson-White syndrome and conduction system disease with onset in childhood and the absence of cardiac hypertrophy.

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