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Exome sequencing in Asian populations identifies low-frequency and rare coding variation influencing Parkinson's disease risk.
Chew EG, Liu Z, Li Z, Chung SJ, Lian MM, Tandiono M, Heng YJ, Ng EY, Tan LC, Chng WL, Tan TJ, Peh EK, Ho YS, Chen XY, Lim EY, Chang CH, Leong JJ, Peh TX, Chan LL, Chao Y, Au WL, Prakash KM, Lim JL, Tay YW, Mok V, Chan AY, Lin JJ, Jeon BS, Song K, Tham CC, Pang CP, Ahn J, Park KH, Wiggs JL, Aung T, Tan AH, Ahmad Annuar A, Makarious MB, Blauwendraat C, Nalls MA, Robak LA, Alcalay RN, Gan-Or Z, Reynolds R, Lim SY, Xia Y, Khor CC, Tan EK, Wang Z, Foo JN. Chew EG, et al. Among authors: lim sy. Nat Aging. 2024 Nov 21. doi: 10.1038/s43587-024-00760-7. Online ahead of print. Nat Aging. 2024. PMID: 39572736
Comprehensive phenotypic assessment of nonsense mutations in mitochondrial ND5 in mice.
Kim S, Park SG, Kim J, Hong S, Cho SM, Lim SY, Kim EK, Ju S, Lee SB, Kim SP, Jeong TY, Oh Y, Han S, Kim HR, Lee TC, Kim HC, Yoon WK, An TH, Oh KJ, Nam KH, Lee S, Kim K, Seong JK, Lee H. Kim S, et al. Among authors: lim sy. Exp Mol Med. 2024 Nov 1. doi: 10.1038/s12276-024-01333-9. Online ahead of print. Exp Mol Med. 2024. PMID: 39482535 Free article.
1,474 results