Ippel, E.F.

mutation carrier patient family phenotype p.s 13f index patients heart index p.n 342d netherland desmin founder cardiomyopathy myopathy dutch block right atrioventricular block p.n 342d carriers conduction analysis disease abnormality cardiological haplotype analysis conduction disease table obligate haplotype p.s 13f carriers pacemaker university screening information distribution symptom atrioventricular des mutations heart failure enlargement symbol centre department des mutation carriers p.s 13f mutation flexor failure collapse family cascade screening domain study 2 b domain death dutch families article cardiomyopathic phenotype founder effects repolarisation n 342d utrecht o-iii genealogy ventricle dysfunction pedigree individual u-iii disorder groningen weakness bulbar muscle cardiological symptoms conduction disorders region microsatellite markers pacemaker therapy characteristic cardioverter defibrillator