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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 11, 2023. (Total: 223939Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Atrial Fibrillation and SCN1B[original query]
Mutations in sodium channel ß1- and ß2-subunits associated with atrial fibrillation.
Circulation. Arrhythmia and electrophysiology 2009 Jun 2 (3): 268-75.
Watanabe Hiroshi, Darbar Dawood, Kaiser Daniel W, Jiramongkolchai Kim, Chopra Sameer, Donahue Brian S, Kannankeril Prince J, Roden Dan
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
Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation.
Circulation. Arrhythmia and electrophysiology 2015 Jun .
Hayashi Kenshi, Konno Tetsuo, Tada Hayato, Tani Satoyuki, Liu Li, Fujino Noboru, Nohara Atsushi, Hodatsu Akihiko, Tsuda Toyonobu, Tanaka Yoshihiro, Kawashiri Masa-Aki, Ino Hidekazu, Makita Naomasa, Yamagishi Masaka
Rare variants in genes encoding the cardiac sodium channel and associated compounds and their impact on outcome of catheter ablation of atrial fibrillation.
PloS one 2017 8 12 (8): e0183690.
Husser Daniela, Ueberham Laura, Hindricks Gerhard, Büttner Petra, Ingram Christie, Weeke Peter, Shoemaker M Benjamin, Adams Volker, Arya Arash, Sommer Philipp, Darbar Dawood, Roden Dan M, Bollmann Andre
A Novel PITX2c Gain-of-Function Mutation, p.Met207Val, in Patients With Familial Atrial Fibrillation.
The American journal of cardiology 2018 12 123 (5): 787-793.
Mechakra Asma, Footz Tim, Walter Michael, Aránega Amelia, Hernández-Torres Francisco, Morel Elodie, Millat Gilles, Yang Yi-Qing, Chahine Mohamed, Chevalier Philippe, Christé Georg
Significant association of rare variant p.Gly8Ser in cardiac sodium channel ?4-subunit SCN4B with atrial fibrillation.
Annals of human genetics 2019 3 83 (4): 239-248.
Xiong Hongbo, Yang Qin, Zhang Xiaoping, Wang Pengxia, Chen Feifei, Liu Ying, Wang Pengyun, Zhao Yuanyuan, Li Sisi, Huang Yufeng, Chen Shanshan, Wang Xiaojing, Zhang Hongfu, Yu Dong, Tan Chencheng, Fang Cheng, Huang Yuan, Wu Gang, Wu Yanxia, Cheng Xiang, Liao Yuhua, Zhang Rongfeng, Yang Yanzong, Ke Tie, Ren Xiang, Li Hui, Tu Xin, Xia Yunlong, Xu Chengqi, Chen Qiuyun, Wang Qing
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