Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: CTTNBP2[original query] |
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Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population.
Journal of lipid research 2018 Aug . Hebbar Prashantha, Nizam Rasheeba, Melhem Motasem, Alkayal Fadi, Elkum Naser, John Sumi Elsa, Tuomilehto Jaakko, Alsmadi Osama, Thanaraj Thangavel Alphon |
Coding mutations in NUS1 contribute to Parkinson's disease. Proceedings of the National Academy of Sciences of the United States of America 2018 10 115 (45): 11567-11572. Guo Ji-Feng, Zhang Lu, Li Kai, Mei Jun-Pu, Xue Jin, Chen Jia, Tang Xia, Shen Lu, Jiang Hong, Chen Chao, Guo Hui, Wu Xue-Li, Sun Si-Long, Xu Qian, Sun Qi-Ying, Chan Piu, Shang Hui-Fang, Wang Tao, Zhao Guo-Hua, Liu Jing-Yu, Xie Xue-Feng, Jiang Yi-Qi, Liu Zhen-Hua, Zhao Yu-Wen, Zhu Zuo-Bin, Li Jia-da, Hu Zheng-Mao, Yan Xin-Xiang, Fang Xiao-Dong, Wang Guang-Hui, Zhang Feng-Yu, Xia Kun, Liu Chun-Yu, Zhu Xiong-Wei, Yue Zhen-Yu, Li Shuai Cheng, Cai Huai-Bin, Zhang Zhuo-Hua, Duan Ran-Hui, Tang Bei-S |
Identification of a novel large deletion and other copy number variations in the CFTR gene in patients with Cystic Fibrosis from a multiethnic population. Molecular genetics & genomic medicine 2019 6 7 (7): e00645. Martins Raisa da Silva, Campos Junior Mario, Dos Santos Moreira Aline, Marques Zembrzuski Verônica, da Fonseca Ana Carolina Proença, Abreu Gabriella de Medeiros, Cabello Pedro Hernan, de Cabello Giselda Maria Kal |
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