Paradigm of Genetic Mosaicism and Lone Atrial Fibrillation
Author(s) -
Isabelle Thibodeau,
Ji Xu,
Qiuju Li,
Gele Liu,
Khanh Lam,
John P. Veinot,
David Birnie,
Douglas L. Jones,
Andrew D. Krahn,
Robert Lemery,
Bruce J. Nicholson,
Michael H. Gollob
Publication year - 2010
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/circulationaha.110.961227
Subject(s) - frameshift mutation , genetics , mutation , connexin , medicine , biology , gene , gap junction , intracellular
Atrial fibrillation (AF) is the most common sustained arrhythmia observed in otherwise healthy individuals. Most lone AF cases are nonfamilial, leading to the assumption that a primary genetic origin is unlikely. In this study, we provide data supporting a novel paradigm that atrial tissue-specific genetic defects may be associated with sporadic cases of lone AF.
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