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| 臺大學術典藏 |
2018-09-10T15:33:08Z |
Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation
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Hsieh, Chia-Shan; Chang, Sheng-Nan; Chuang, Eric Y.; Ueng, Kwo-Chang; Tsai, Chin-Feng; Lin, Tsung-Hsien; Wu, Cho-Kai; Lee, Jen-Kuang; Lin, Lian-Yu; Wang, Yi-Chih; Yu, Chih-Chieh; Lai, Ling-Ping; Tseng, Chuen-Den; Hwang, Juey-Jen; Chiang, Fu-Tien; Lin, Jiunn-Lee; Tsai, Chia-Ti; CHO-KAI WU; Tsai, Chia-Ti; SHENG NAN CHANG; JUEY-JEN HWANG; FU-TIEN CHIANG; LING-PING LAI; LIAN-YU LIN; Lin, Tsung-Hsien; CHIH-CHIEH YU; YI-CHIH WANG; Lin, Jiunn-Lee et al. |
| 臺大學術典藏 |
2018-09-10T15:01:03Z |
Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome
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Lu, Tzu-Pin; Lai, Liang-Chuan; Ho, Chia-Chuan; Liu, Yen-Bin; Tsai, Chia-Ti; Lin, Lian-Yu; Yu, Chih-Chieh; Chen, Wen-Jone; Chiang, Fu-Tien; Yeh, Shih-Fan Sherri; Lai, Ling-Ping; Chuang, Eric Y.; Lin, Jiunn-Lee; Juang, Jyh-Ming Jimmy; Juang, Jyh-Ming Jimmy; T.-P. LU; LIANG-CHUAN LAI; FU-TIEN CHIANG; LING-PING LAI; Liu, Yen-Bin; LIAN-YU LIN; Tsai, Chia-Ti; CHIH-CHIEH YU; ERIC YAO-YU CHUANG; Lin, Jiunn-Lee et al. |
Showing items 1-2 of 2 (1 Page(s) Totally)
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