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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Nov 8, 2024. (Total: 233355Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Arrhythmia and SCN3B[original query]
Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population.
Biochemical and biophysical research communications 2010 Jul 398 (1): 98-104.
Wang Pengyun, Yang Qinbo, Wu Xiaofen, Yang Yanzong, Shi Lisong, Wang Chuchu, Wu Gang, Xia Yunlong, Yang Bo, Zhang Rongfeng, Xu Chengqi, Cheng Xiang, Li Sisi, Zhao Yuanyuan, Fu Fenfen, Liao Yuhua, Fang Fang, Chen Qiuyun, Tu Xin, Wang Qing
Mutations in sodium channel ß-subunit SCN3B are associated with early-onset lone atrial fibrillation.
Cardiovascular research 2011 Mar 89 (4): 786-93.
Olesen Morten S, Jespersen Thomas, Nielsen Jonas B, Liang Bo, Møller Daniel V, Hedley Paula, Christiansen Michael, Varró András, Olesen Søren-Peter, Haunsø Stig, Schmitt Nicole, Svendsen Jesper
Novel SCN3B mutation associated with brugada syndrome affects intracellular trafficking and function of Nav1.5.
Circulation journal : official journal of the Japanese Circulation Society 2012 Dec .
Ishikawa T, Takahashi N, Ohno S, Sakurada H, Nakamura K, On YK, Park JE, Makiyama T, Horie M, Arimura T, Makita N, Kimura A
Sodium current and potassium transient outward current genes in Brugada syndrome: screening and bioinformatics.
The Canadian journal of cardiology 0 28 (2): 196-200.
Holst Anders G, Saber Siamak, Houshmand Massoud, Zaklyazminskaya Elena V, Wang Yinman, Jensen Henrik Kjærulf, Refsgaard Lena, Haunsø Stig, Svendsen Jesper Hastrup, Olesen Morten S, Tfelt-Hansen Jac
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