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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: chen l, chen w. 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.
GGC Repeat Expansion of RILPL1 is Associated with Oculopharyngodistal Myopathy.
Zeng YH, Yang K, Du GQ, Chen YK, Cao CY, Qiu YS, He J, Lv HD, Qu QQ, Chen JN, Xu GR, Chen L, Zheng FZ, Zhao M, Lin MT, Chen WJ, Hu J, Wang ZQ, Wang N. Zeng YH, et al. Among authors: chen l, chen jn, chen yk, chen wj. Ann Neurol. 2022 Sep;92(3):512-526. doi: 10.1002/ana.26436. Epub 2022 Jul 2. Ann Neurol. 2022. PMID: 35700120
Correction of human nonsense mutation via adenine base editing for Duchenne muscular dystrophy treatment in mouse.
Jin M, Lin J, Li H, Li Z, Yang D, Wang Y, Yu Y, Shao Z, Chen L, Wang Z, Zhang Y, Zhang X, Wang N, Xu C, Yang H, Chen WJ, Li G. Jin M, et al. Among authors: chen l, chen wj. Mol Ther Nucleic Acids. 2024 Mar 6;35(2):102165. doi: 10.1016/j.omtn.2024.102165. eCollection 2024 Jun 11. Mol Ther Nucleic Acids. 2024. PMID: 38571746 Free PMC article.
Detection of pTDP-43 via routine muscle biopsy: A promising diagnostic biomarker for amyotrophic lateral sclerosis.
Zhang QJ, Lin J, Wang YL, Chen L, Ding Y, Zheng FZ, Song HH, Lv AW, Li YY, Guo QF, Lin MT, Hu W, Xu LQ, Zhao WL, Fang L, Cui MC, Fu ZF, Chen WJ, Zhang J, Wang ZQ, Wang N, Fu Y. Zhang QJ, et al. Among authors: chen l, chen wj. Brain Pathol. 2024 Apr 11:e13261. doi: 10.1111/bpa.13261. Online ahead of print. Brain Pathol. 2024. PMID: 38602336
82,459 results
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