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Autosomal dominant Parkinson's disease caused by the recently identified LRRK2 N1437D mutation in a Chinese family: Clinical features, imaging findings, and functional impact.
Sun YM, Gan LH, Peng F, Zhou XY, Chen QS, Liu FT, Tang YL, Wu P, Lu JY, Ge JJ, Yen TC, Zuo CT, Song B, Wu JJ, Wang J. Sun YM, et al. Parkinsonism Relat Disord. 2023 Jun;111:105441. doi: 10.1016/j.parkreldis.2023.105441. Epub 2023 May 12. Parkinsonism Relat Disord. 2023. PMID: 37201327
Olfaction in Parkin carriers in Chinese patients with Parkinson disease.
Wang Y, Wu JJ, Liu FT, Chen K, Chen C, Luo SS, Wang YX, Li DK, Guan RY, Yang YJ, An Y, Wang J, Sun YM. Wang Y, et al. Among authors: sun ym. Brain Behav. 2017 Mar 28;7(5):e00680. doi: 10.1002/brb3.680. eCollection 2017 May. Brain Behav. 2017. PMID: 28523222 Free PMC article.
693 results