Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Disease and SLC10A1[original query] |
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| Comprehensive assessment showed no associations of variants at the SLC10A1 locus with susceptibility to persistent HBV infection among Southern Chinese. Scientific reports 2017 Apr 7 46490. Zhang Ying, Li Yuanfeng, Wu Miantao, Cao Pengbo, Liu Xiaomin, Ren Qian, Zhai Yun, Xie Bobo, Hu Yanling, Hu Zhibin, Bei Jinxin, Ping Jie, Liu Xinyi, Yu Yinghua, Guo Bingqian, Lu Hui, Liu Guanjun, Zhang Haitao, Cui Ying, Mo Zengnan, Shen Hongbing, Zeng Yi-Xin, He Fuchu, Zhang Hongxing, Zhou Gangqi |
| SLC10A1 rs2296651 variant (S267F mutation) predicts biochemical traits, hepatitis B virus infection susceptibility and the risk of gallstone disease. Molecular genetics and genomics : MGG 2024 6 299 (1): 62. Yu-Lin Ko, Wei-Lun Tuan, Ming-Sheng Teng, Wei-Chih Su, Chia-Chi Wang, Leay-Kiaw Er, Semon Wu, Lung-An H |
| Genetic variation features of neonatal hyperbilirubinemia caused by inherited diseases. World journal of clinical pediatrics 2024 12 13 (4): 98462. Jin-Ying You, Ling-Yun Xiong, Min-Fang Wu, Jun-Song Fan, Qi-Hua Fu, Ming-Hua Q |
- Page last reviewed:Feb 1, 2024
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