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Association of TRMT2B gene variants with juvenile amyotrophic lateral sclerosis.
Liu Y, He X, Yuan Y, Li B, Liu Z, Li W, Li K, Tan S, Zhu Q, Tang Z, Han F, Wu Z, Shen L, Jiang H, Tang B, Qiu J, Hu Z, Wang J. Liu Y, et al. Among authors: li w, li k, li b. Front Med. 2024 Feb;18(1):68-80. doi: 10.1007/s11684-023-1005-y. Epub 2023 Oct 24. Front Med. 2024. PMID: 37874476
HCFC1 variants in the proteolysis domain are associated with X-linked idiopathic partial epilepsy: Exploring the underlying mechanism.
He N, Guan BZ, Wang J, Liu HK, Mao Y, Liu ZG, Yin F, Peng J, Xiao B, Tang BS, Zhou D, Huang G, Dai QL, Zeng Y, Han H, Zhai QX, Li B, Tang B, Li WB, Song W, Liu L, Shi YW, Li BM, Su T, Zhou P, Liu XR, Guo LW, Yi YH, Liao WP. He N, et al. Among authors: li wb, li bm, li b. Clin Transl Med. 2023 Jun;13(6):e1289. doi: 10.1002/ctm2.1289. Clin Transl Med. 2023. PMID: 37264743 Free PMC article.
Interactions of genetic risks for autism and the broad autism phenotypes.
Dong L, Wang Y, Wang X, Luo T, Zhou Q, Zhao G, Li B, Xia L, Xia K, Li J. Dong L, et al. Among authors: li j, li b. Front Psychiatry. 2023 Mar 21;14:1110080. doi: 10.3389/fpsyt.2023.1110080. eCollection 2023. Front Psychiatry. 2023. PMID: 37102084 Free PMC article.
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