The genetic puzzle of familial atrial fibrillation
AAY Ragab, GDS Sitorus, BB Brundel… - Frontiers in …, 2020 - frontiersin.org
… Atrial fibrillation (AF) is the most common clinical tachyarrhythmia. In Europe, AF is expected
… investigated in depth since the first report of familial atrial fibrillation (FAF) in 1936. Despite …
… investigated in depth since the first report of familial atrial fibrillation (FAF) in 1936. Despite …
Identification of a genetic locus for familial atrial fibrillation
R Brugada, T Tapscott… - … England Journal of …, 1997 - Mass Medical Soc
… responsible for a familial form of the disease. Familial atrial fibrillation is probably very
uncommon, 5 but we located a small family in Spain in which atrial fibrillation segregates as an …
uncommon, 5 but we located a small family in Spain in which atrial fibrillation segregates as an …
Association between familial atrial fibrillation and risk of new-onset atrial fibrillation
… %) and premature familial AF occurred among 351 participants (7.9%). Atrial fibrillation
occurred more frequently among participants with familial AF than without familial AF (unadjusted …
occurred more frequently among participants with familial AF than without familial AF (unadjusted …
Familial atrial fibrillation is a genetically heterogeneous disorder
D Darbar, KJ Herron, JD Ballew, A Jahangir… - Journal of the American …, 2003 - jacc.org
… The aims of this study were to identify and characterize familial cases of atrial fibrillation (AF)
in our clinical practice and to determine whether AF is genetically heterogeneous. …
in our clinical practice and to determine whether AF is genetically heterogeneous. …
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Genetics of familial atrial fibrillation
O Campuzano, R Brugada - Europace, 2009 - academic.oup.com
… Atrial fibrillation (AF) remains one of the most common and challenging arrhythmias encountered
in clinical practice. While familial … the arrhythmia. Despite the limited prevalence of the …
in clinical practice. While familial … the arrhythmia. Despite the limited prevalence of the …
Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation
DM Hodgson-Zingman, ML Karst… - … England Journal of …, 2008 - Mass Medical Soc
… To elucidate the mechanism by which a mutation in NPPA could lead to familial atrial
fibrillation, we first showed that the mutation we identified results in the production of a mutant …
fibrillation, we first showed that the mutation we identified results in the production of a mutant …
A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation
N Orr, R Arnaout, LJ Gula, DA Spears… - Nature …, 2016 - nature.com
Atrial fibrillation (AF), the most common arrhythmia, is a growing epidemic with substantial
morbidity and economic burden. Mechanisms underlying vulnerability to AF remain poorly …
morbidity and economic burden. Mechanisms underlying vulnerability to AF remain poorly …
Novel connexin40 missense mutations in patients with familial atrial fibrillation
YQ Yang, X Liu, XL Zhang, XH Wang, HW Tan… - Europace, 2010 - academic.oup.com
Aims This research was aimed at screening connexin40, a cardiac gap junction protein alpha
5, for genetic defects in patients with familial atrial fibrillation (AF). Methods The subjects …
5, for genetic defects in patients with familial atrial fibrillation (AF). Methods The subjects …
KCNQ1 gain-of-function mutation in familial atrial fibrillation
YH Chen, SJ Xu, S Bendahhou, XL Wang, Y Wang… - Science, 2003 - science.org
… Atrial fibrillation can occur on a familial basis, pointing to a genetic cause of the arrhythmia
in some individuals. Hereditary AF in three families was recently linked to a locus between …
in some individuals. Hereditary AF in three families was recently linked to a locus between …
Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation
Y Yang, M Xia, Q Jin, S Bendahhou, J Shi… - The American Journal of …, 2004 - cell.com
Atrial fibrillation (AF) is the most common cardiac arrhythmia encountered in clinical practice.
We first reported an S140G mutation of KCNQ1, an α subunit of potassium channels, in one …
We first reported an S140G mutation of KCNQ1, an α subunit of potassium channels, in one …