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The genetic spectrum of LRRK2 variants in Parkinson's disease: findings from a large Chinese cohort.

Wan J, Pan H, Chang D, Zhao Y, Xu Q, Yao L, Sun Q, Zhang X, He R, Wang C, Zhang H, Lei L, Wang Y, Li M, Wu H, Ma J, Wu Y, Xu Y, Xiong N, Wang T, Wang X, Chen L, Xu Y, Cao H, Zhang K, Liu W, Zhang Y, Mao C, Wang Q, Xue Z, Zhang Z, Cheng O, Huang W, Zhao G, Cui G, Chen T, Wang P, Di W, Liu H, Zheng H, Chen C, Guo H, Xia K, Zhang Z, Yuan K, Li J, Wang J, Guo J, Shen L, Jiang H, Liu C, Liu J, Chan P, Liu Z, Tang B, Parkinson’s Disease & Movement Disorders Multicenter Database and Collaborative Network in China (PD-MDCNC), China Essential Tremor Alliance (CETA).

NPJ Parkinsons Dis · 2026-03-28

DOI: 10.1038/s41531-026-01315-wPMID: 41904258

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.
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Identification of Parkinson’s disease-associated regulatory variants in human dopaminergic neurons reveals modulators of <i>SCARB2</i> and <i>BAG3</i> expression

Gérard D, Ohnmacht J, Gomez-Ramos B, Catillon M, Sharif J, Baumgarten N, Hecker D, Ginolhac A, Landoulsi Z, Valceschini E, Rakovic A, Klein C, May P, Koseki H, Schulz MH, Sauter T, Krüger R, Sinkkonen L.

· 2026-03-27

DOI: 10.64898/2026.03.26.714241

A bibliographic record traceable to Europe PMC. Türkçe başlık: makine çevirisi, editoryal kontrol bekliyor.

Records come from scientific sources. Bibliographic counts do not represent completed translations or editorial approvals.

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