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Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy.
Zheng F, Qiu L, Chen L, Zheng Y, Lin X, He J, Lin X, He Q, Lin Y, Lin L, Wang L, Lin F, Yang K, Lin M, Lin Y, Fu Y, Wang N, Wang Z. Zheng F, et al. Among authors: lin f, lin y, lin x, lin m, lin l. Neurology. 2023 Jul 18;101(3):e225-e237. doi: 10.1212/WNL.0000000000207418. Epub 2023 May 24. Neurology. 2023. PMID: 37225433 Free PMC article.
Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study.
Wang Z, Qiu L, Lin M, Chen L, Zheng F, Lin L, Lin F, Ye Z, Lin X, He J, Wang L, Lin X, He Q, Chen W, Lin Y, Fu Y, Wang N. Wang Z, et al. Among authors: lin f, lin y, lin x, lin m, lin l. Lancet Reg Health West Pac. 2021 Nov 22;18:100323. doi: 10.1016/j.lanwpc.2021.100323. eCollection 2022 Jan. Lancet Reg Health West Pac. 2021. PMID: 35024656 Free PMC article.
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