[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 …

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 …

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 …

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 …

Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation

IE Christophersen, MS Olesen, B Liang… - European heart …, 2013 - academic.oup.com
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 …

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 …

[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 …

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 …

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 …

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 …