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DYNC1H1-related epilepsy: Genotype-phenotype correlation.
Liu W, Cheng M, Zhu Y, Chen Y, Yang Y, Chen H, Niu X, Tian X, Yang X, Zhang Y. Liu W, et al. Among authors: tian x. Dev Med Child Neurol. 2023 Apr;65(4):534-543. doi: 10.1111/dmcn.15414. Epub 2022 Sep 29. Dev Med Child Neurol. 2023. PMID: 36175372 Free article.
[Analysis of SCN1A deletions or duplications in patients with Dravet syndrome].
Zeng Q, Zhang Y, Yang X, Xu X, Zhang J, Tian X, Liu A, Liu X, Jiang Y, Wu X. Zeng Q, et al. Among authors: tian x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Dec 10;34(6):787-791. doi: 10.3760/cma.j.issn.1003-9406.2017.06.001. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 29188601 Chinese.
Phenotypic Spectrum and Prognosis of Epilepsy Patients With GABRG2 Variants.
Yang Y, Niu X, Cheng M, Zeng Q, Deng J, Tian X, Wang Y, Yu J, Shi W, Wu W, Ma J, Li Y, Yang X, Zhang X, Jia T, Yang Z, Liao J, Sun Y, Zheng H, Sun S, Sun D, Jiang Y, Zhang Y. Yang Y, et al. Among authors: tian x. Front Mol Neurosci. 2022 Mar 14;15:809163. doi: 10.3389/fnmol.2022.809163. eCollection 2022. Front Mol Neurosci. 2022. PMID: 35359574 Free PMC article.
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