Open AccessVariable primary phenotypic manifestations in a rare familial form of Wolff–Parkinson–White syndrome and hypertrophic cardiomyopathy
Author(s) -
Katrine M. Müllertz,
Henrik Kjærulf Jensen
Publication year - 2015
Publication title -
ep europace
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.119
H-Index - 102
eISSN - 1532-2092
pISSN - 1099-5129
DOI - 10.1093/europace/euv221
Subject(s) - proband , daughter , white (mutation) , medicine , cardiomyopathy , cardiology , phenotype , atrial fibrillation , heart block , heart failure , genetics , electrocardiography , mutation , gene , biology , evolutionary biology
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