[PDF][PDF] A Novel KCNQ1 Missense Mutation Identified in a Patient with Juvenile-Onset
H Itoh - niigata-u.repo.nii.ac.jp
Background: Atrial fibrillation (AF) is one of the most common cardiac arrhythmias, and in
some patients, the disease is inheritable. Hereditary aspects of AF, however, remain not fully …
some patients, the disease is inheritable. Hereditary aspects of AF, however, remain not fully …
Novel KCNQ1 Missense Mutation Associated with Juvenile-Onset Atrial Fibrillation
K Hasegawa, S Ohno, H Itoh, T Hattori, T Makiyama… - 2012 - Am Heart Assoc
Introduction; Atrial fibrillation (AF) is the most common cardiac arrhythmia occurring in the
general population. Recently, several gene mutations associated with ion channels were …
general population. Recently, several gene mutations associated with ion channels were …
A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels
K Hasegawa, S Ohno, T Ashihara, H Itoh, WG Ding… - Heart Rhythm, 2014 - Elsevier
Background Atrial fibrillation (AF) is one of the most common cardiac arrhythmias. In some
patients, the disease is inheritable; however, hereditary aspects of AF remain not fully …
patients, the disease is inheritable; however, hereditary aspects of AF remain not fully …
Molecular genetic analysis of six Dutch families with atrial fibrillation
MM Entius, A Groenewegen, A Pronk… - Netherlands Heart …, 2005 - ncbi.nlm.nih.gov
Background Atrial fibrillation (AF), the most common cardiac arrhythmia, is characterised by
rapid and irregular contraction of the atrium. The risk of AF increases with age and AF …
rapid and irregular contraction of the atrium. The risk of AF increases with age and AF …
Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation
Aims Genetic factors may be important in the development of atrial fibrillation (AF) in the
young. KCNA5 encodes the potassium channel α-subunit KV1. 5, which underlies the …
young. KCNA5 encodes the potassium channel α-subunit KV1. 5, which underlies the …
KCNQ1 Gain-of-function Mutation Associated With Familial Atrial Fibrillation
D Darbar, R Abraham, G Kucera, T Stubblefield… - 2007 - Am Heart Assoc
Background: Family history is a risk factor for atrial fibrillation (AF). We report here a 3-
generation Caucasian family with familial AF and a highly dysfunctional mutation in KCNQ1 …
generation Caucasian family with familial AF and a highly dysfunctional mutation in KCNQ1 …
[PDF][PDF] 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 …
KCNQ1 and KCNE3 Mutations Associated with Atrial Fibrillation
TE Rhodes, LJ Manderfield, AL Lundquist… - 2006 - Am Heart Assoc
Susceptibility to atrial fibrillation (AF) may have a genetic etiology as evidenced by the
association of familial AF with mutations in KCNQ1 and other genes. We re-sequenced …
association of familial AF with mutations in KCNQ1 and other genes. We re-sequenced …
Atrial Fibrillation Genetic Considerations: The Basic Scientist's Perspective
QK Wang - Atrial Fibrillation: From Bench to Bedside, 2008 - Springer
Common atrial fibrillation (AF) is a complex disease, and its pathogenesis involves multiple
genetic factors, environmental factors, and interactions among these factors. Genetic factors …
genetic factors, environmental factors, and interactions among these factors. Genetic factors …
Direct Evidence that a KCNQ1 Mutation is Linked to Familial Early-onset Atrial Fibrillation
DC Bartos, JB Anderson, R Bastiaenen, JN Johnson… - 2012 - Am Heart Assoc
KCNQ1 encodes the voltage-gated α-subunit of the IKs channel complex (Kv7. 1), and
KCNQ1 mutations are associated with multiple arrhythmia syndromes. Over the past 12 …
KCNQ1 mutations are associated with multiple arrhythmia syndromes. Over the past 12 …