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Circulation. Arrhythmia and Electrophysiology|April 16, 2011
KCNE5 (KCNE1L) variants are novel modulators of Brugada syndrome and idiopathic ventricular fibrillationSeiko Ohno, Dimitar P Zankov, Wei-Guang Ding, et al.
International Journal of Cardiology|August 12, 2008
A novel KCNH2 mutation as a modifier for short QT intervalHideki Itoh, Tomoko Sakaguchi, Takashi Ashihara, et al.
Journal of Cardiology|November 18, 2017
Novel intracellular transport-refractory mutations in KCNH2 identified in patients with symptomatic long QT syndromeDaisuke Fukumoto, Wei-Guang Ding, Yuko Wada, et al.
Journal of Cardiovascular Electrophysiology|January 10, 2014
Gain-of-function KCNH2 mutations in patients with Brugada syndromeQ I Wang, Seiko Ohno, Wei-Guang Ding, et al.
Journal of the American College of Cardiology|August 22, 2009
D85N, a KCNE1 polymorphism, is a disease-causing gene variant in long QT syndromeYukiko Nishio, Takeru Makiyama, Hideki Itoh, et al.
Heart Rhythm|January 1, 2010
KCNE2 modulation of Kv4.3 current and its potential role in fatal rhythm disordersJie Wu, Wataru Shimizu, Wei-Guang Ding, et al.
Circulation. Cardiovascular Genetics|May 17, 2012
Phenotype variability in patients carrying KCNJ2 mutationsHiromi Kimura, Jun Zhou, Mihoko Kawamura, et al.
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