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Rare KCND3 Loss-of-Function Mutation Associated With the SCA19/22.
Li M, Liu F, Hao X, Fan Y, Li J, Hu Z, Shi J, Fan L, Zhang S, Ma D, Guo M, Xu Y, Shi C. Li M, et al. Among authors: liu f. Front Mol Neurosci. 2022 Jun 23;15:919199. doi: 10.3389/fnmol.2022.919199. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35813061 Free PMC article.
ARSA gene variants and Parkinson's disease.
Fan Y, Mao CY, Dong YL, Shen S, Zhang QM, Yao DB, Liu F, Li MJ, Hu XC, Wang T, Liu YT, Liu H, Wang YL, Yuan YP, Zhang C, Yang J, Shi CH, Xu YM. Fan Y, et al. Among authors: liu h, liu yt, liu f. Brain. 2020 Jun 1;143(6):e47. doi: 10.1093/brain/awaa134. Brain. 2020. PMID: 32437521 No abstract available.
Generation of an induced pluripotent stem cell line (ZZUi020-A) from a patient with Parkinson's disease harboring the intermediate-length GGC repeat expansions in the NOTCH2NLC gene.
Fan Y, Liu F, Fan LY, Mao CY, Liu H, Zhang C, Yuan YP, Yang J, Wang YL, Liu YT, Shi CH, Xu YM. Fan Y, et al. Among authors: liu h, liu yt, liu f. Stem Cell Res. 2021 Apr;52:102257. doi: 10.1016/j.scr.2021.102257. Epub 2021 Feb 18. Stem Cell Res. 2021. PMID: 33626493 Free article.
GIPC1 CGG Repeat Expansion Is Associated with Movement Disorders.
Fan Y, Shen S, Yang J, Yao D, Li M, Mao C, Wang Y, Hao X, Ma D, Li J, Shi J, Guo M, Li S, Yuan Y, Liu F, Yang Z, Zhang S, Hu Z, Fan L, Liu H, Zhang C, Wang Y, Wang Q, Zheng H, He Y, Song B, Xu Y, Shi C. Fan Y, et al. Among authors: liu h, liu f. Ann Neurol. 2022 May;91(5):704-715. doi: 10.1002/ana.26325. Epub 2022 Mar 8. Ann Neurol. 2022. PMID: 35152460
36,298 results
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