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Coding mutations in NUS1 contribute to Parkinson's disease.
Guo JF, Zhang L, Li K, Mei JP, Xue J, Chen J, Tang X, Shen L, Jiang H, Chen C, Guo H, Wu XL, Sun SL, Xu Q, Sun QY, Chan P, Shang HF, Wang T, Zhao GH, Liu JY, Xie XF, Jiang YQ, Liu ZH, Zhao YW, Zhu ZB, Li JD, Hu ZM, Yan XX, Fang XD, Wang GH, Zhang FY, Xia K, Liu CY, Zhu XW, Yue ZY, Li SC, Cai HB, Zhang ZH, Duan RH, Tang BS. Guo JF, et al. Among authors: zhao yw, zhao gh. Proc Natl Acad Sci U S A. 2018 Nov 6;115(45):11567-11572. doi: 10.1073/pnas.1809969115. Epub 2018 Oct 22. Proc Natl Acad Sci U S A. 2018. PMID: 30348779 Free PMC article.
Rare GCH1 heterozygous variants contributing to Parkinson's disease.
Xu Q, Li K, Sun Q, Ding D, Zhao Y, Yang N, Luo Y, Liu Z, Zhang Y, Wang C, Xia K, Yan X, Jiang H, Shen L, Tang B, Guo J. Xu Q, et al. Brain. 2017 Jul 1;140(7):e41. doi: 10.1093/brain/awx110. Brain. 2017. PMID: 28582483 No abstract available.
[Progress in genetic research on essential tremor].
Zhao Y, Sun Q, Li K, Guo J, Tang B, Yan X. Zhao Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Oct 10;34(5):767-771. doi: 10.3760/cma.j.issn.1003-9406.2017.05.032. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28981951 Review. Chinese.
240 results