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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. Among authors: wu jj, wu p. Parkinsonism Relat Disord. 2023 Jun;111:105441. doi: 10.1016/j.parkreldis.2023.105441. Epub 2023 May 12. Parkinsonism Relat Disord. 2023. PMID: 37201327
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