BookH.F. Baars, J.J. van der Smagt, P. Doevandans.
Contents:
Introduction to molecular genetics
Clinical genetics
Hypertrophic cardiomyopathy
Familial dilated cardiomyopathy
Arrhythmogenic right ventricular dysplasia/cardiomyopathy from desmosome to disease
Noncompaction cardiomyopathy
Mitochondrial cardiomyopathy
Restrictive cardiomyopathy
Congenital long QT-syndrome
The Brugada syndrome
Short QT syndrome
Catecholaminergic polymorphic ventricular tachycardia
A molecular genetic perspective on atrial fibrillation
Idiopathic ventricular fibrillation
The genetics of mitral valve prolapse
Atrioventricular (AV) reentry tachycardia
Hereditary cardiac conduction diseases
Connective tissue disorders and smooth muscle disorders in cardiology
Genetics of congenital heart defects
Genetic disorders of the lipoprotein metabolism: diagnosis and management
Novel insights into genetics of arterial thrombosis
The pharmacogenetics of atherosclerosis
Genetics of (premature) coronary artery disease
Heredity neuromuscular diseases and cardiac involvement
Sudden cardiac death in the young: epidemiology and cardiogenetic evaluation of victims and their relatives
The outpatient clinics for cardiogenetics
Abdominal aortic aneurysm
Future of cardiogenetics.