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Page 1
The mutation spectrum of Parkinson-disease-related genes in early-onset Parkinson's disease in ethnic Chinese.
Chen YP, Yu SH, Zhang GH, Hou YB, Gu XJ, Ou RW, Shen Y, Song W, Chen XP, Zhao B, Cao B, Zhang LY, Sun MM, Liu FF, Wei QQ, Liu KC, Lin JY, Yang TM, Yang J, Wu Y, Jiang Z, Liu J, Cheng YF, Xiao Y, Su WM, Feng F, Cai YY, Li SR, Hu T, Yuan XQ, Zhou QQ, Shao N, Ma S, Shang HF. Chen YP, et al. Eur J Neurol. 2022 Nov;29(11):3218-3228. doi: 10.1111/ene.15509. Epub 2022 Aug 4. Eur J Neurol. 2022. PMID: 35861376
Role of genetics in amyotrophic lateral sclerosis: a large cohort study in Chinese mainland population.
Chen YP, Yu SH, Wei QQ, Cao B, Gu XJ, Chen XP, Song W, Zhao B, Wu Y, Sun MM, Liu FF, Hou YB, Ou RW, Zhang LY, Liu KC, Lin JY, Xu XR, Li CY, Yang J, Jiang Z, Liu J, Cheng YF, Xiao Y, Chen K, Feng F, Cai YY, Li SR, Hu T, Yuan XQ, Guo XY, Liu H, Han Q, Zhou QQ, Shao N, Li JP, Pan PL, Ma S, Shang HF. Chen YP, et al. J Med Genet. 2022 Sep;59(9):840-849. doi: 10.1136/jmedgenet-2021-107965. Epub 2021 Sep 20. J Med Genet. 2022. PMID: 34544842 Free PMC article.
RAB32 Variants in a Chinese Parkinson's Disease Cohort.
Wang S, Ou R, Huang J, Lin J, Che N, Yang T, Xiao Y, Jiang Q, Zheng X, Liu J, Li C, Shang H. Wang S, et al. Among authors: lin j. Mov Disord. 2025 Feb;40(2):376-377. doi: 10.1002/mds.30065. Epub 2024 Nov 21. Mov Disord. 2025. PMID: 39569824 No abstract available.
218 results