Syndactyly and long QT syndrome (CaV1.2 missense mutation G406R) is associated with hypertrophic cardiomyopathy

Article ID	Journal	Published Year	Pages	File Type
9169078	Heart Rhythm	2005	4 Pages	PDF

Keywords

CACNA1C Long QT syndrome Sudden death Infants Hypertrophic cardiomyopathy

Related Topics

Health Sciences Medicine and Dentistry Cardiology and Cardiovascular Medicine

Syndactyly and long QT syndrome (CaV1.2 missense mutation G406R) is associated with hypertrophic cardiomyopathy

Authors

Shirley M. MD, Arthur A. MD, PhD, Lieselot MD, PhD, Nico A. MD, PhD,