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Epilepsy-associated genes: an update.
Zhang MW, Liang XY, Wang J, Gao LD, Liao HJ, He YH, Yi YH, He N, Liao WP; China Epilepsy Gene 1.0 Project. Zhang MW, et al. Among authors: wang j. Seizure. 2024 Mar;116:4-13. doi: 10.1016/j.seizure.2023.09.021. Epub 2023 Sep 23. Seizure. 2024. PMID: 37777370
BCOR variants are associated with X-linked recessive partial epilepsy.
Li X, Bian WJ, Liu XR, Wang J, Luo S, Li BM, Yi YH, Wu QY, Zhai QX, Gao LD, Zhang HF, He N, Liao WP; China Epilepsy Gene 1.0 Project. Li X, et al. Among authors: wang j. Epilepsy Res. 2022 Nov;187:107036. doi: 10.1016/j.eplepsyres.2022.107036. Epub 2022 Oct 19. Epilepsy Res. 2022. PMID: 36279688
CELSR1 variants are associated with partial epilepsy of childhood.
Chen Z, Luo S, Liu ZG, Deng YC, He SL, Liu XR, Yi YH, Wang J, Gao LD, Li BM, Wu ZJ, Ye ZL, Liang DH, Bian WJ, Liao WP; China Epilepsy Gene 1.0 Project. Chen Z, et al. Among authors: wang j. Am J Med Genet B Neuropsychiatr Genet. 2022 Oct;189(7-8):247-256. doi: 10.1002/ajmg.b.32916. Epub 2022 Aug 12. Am J Med Genet B Neuropsychiatr Genet. 2022. PMID: 36453712
Variants in BSN gene associated with epilepsy with favourable outcome.
Ye T, Zhang J, Wang J, Lan S, Zeng T, Wang H, He X, Li BM, Deng W, Liao WP, Liu XR. Ye T, et al. Among authors: wang h, wang j. J Med Genet. 2023 Aug;60(8):776-783. doi: 10.1136/jmg-2022-108865. Epub 2022 Dec 12. J Med Genet. 2023. PMID: 36600631 Free PMC article.
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: wang j. Clin Transl Med. 2023 Jun;13(6):e1289. doi: 10.1002/ctm2.1289. Clin Transl Med. 2023. PMID: 37264743 Free PMC article.
202,087 results
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