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Altered structural and functional connectivity in CSF1R-related leukoencephalopathy.
Zhan FX, Zhu ZY, Liu Q, Zhou HY, Luan XH, Huang XJ, Liu XL, Tian WT, Wang SG, Song XX, Chen G, Zhao ML, Wang Y, Tang HD, Hu J, Chen SD, Li BY, Cao L. Zhan FX, et al. Among authors: tian wt. Brain Imaging Behav. 2021 Jun;15(3):1655-1666. doi: 10.1007/s11682-020-00360-0. Brain Imaging Behav. 2021. PMID: 32705467
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.
Yin XM, Lin JH, Cao L, Zhang TM, Zeng S, Zhang KL, Tian WT, Hu ZM, Li N, Wang JL, Guo JF, Wang RX, Xia K, Zhang ZH, Yin F, Peng J, Liao WP, Yi YH, Liu JY, Yang ZX, Chen Z, Mao X, Yan XX, Jiang H, Shen L, Chen SD, Zhang LM, Tang BS. Yin XM, et al. Among authors: tian wt. Hum Mol Genet. 2018 Feb 15;27(4):625-637. doi: 10.1093/hmg/ddx430. Hum Mol Genet. 2018. PMID: 29294000
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.
Yin XM, Lin JH, Cao L, Zhang TM, Zeng S, Zhang KL, Tian WT, Hu ZM, Li N, Wang JL, Guo JF, Wang RX, Xia K, Zhang ZH, Yin F, Peng J, Liao WP, Yi YH, Liu JY, Yang ZX, Chen Z, Mao X, Yan XX, Jiang H, Shen L, Chen SD, Zhang LM, Tang BS. Yin XM, et al. Among authors: tian wt. Hum Mol Genet. 2018 Feb 15;27(4):757-758. doi: 10.1093/hmg/ddy025. Hum Mol Genet. 2018. PMID: 29351621 No abstract available.
Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis.
Xu YQ, Liu XL, Huang XJ, Tian WT, Tang HD, Cao L. Xu YQ, et al. Among authors: tian wt. Chin Med J (Engl). 2018 Feb 20;131(4):477-479. doi: 10.4103/0366-6999.225061. Chin Med J (Engl). 2018. PMID: 29451154 Free PMC article. No abstract available.
62 results