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Cell Biology International|July 29, 2006
Gene delivery into primary cerebral cortical neurons by lentiviral vectorYuzhi Zhang, Hansen Wang, Hong Pan, et al.Minerva Pediatrics|April 9, 2016
Identification of GJC2 gene mutations in Chinese patients with Pelizaeus-Merzbacher-like diseaseTaoyun Ji, Dongxiao Li, Ye Wu, et al.BMC Neurology|December 28, 2013
Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosisXiaoling Yang, Yuehua Zhang, Xiaojing Xu, et al.BMC Medical Genetics|August 31, 2017
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardationQingping Zhang, Jiaping Wang, Jiarui Li, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 11, 2017
Familial cases and male cases with MECP2 mutationsQingping Zhang, Ying Zhao, Xinhua Bao, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 10, 2008
[Analysis of the GABRG2 gene mutation in a Chinese family with generalized epilepsy with febrile seizures plus]Huihui Sun, Yuehua Zhang, Xiaoyan Liu, et al.Plos One|October 28, 2014
Functional study of NIPA2 mutations identified from the patients with childhood absence epilepsyHan Xie, Yuehua Zhang, Pingping Zhang, et al.Seizure|February 19, 2019
Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndromeJiaping Wang, Yongxin Wen, Qingping Zhang, et al.Plos One|May 21, 2014
ATP1A3 mutations and genotype-phenotype correlation of alternating hemiplegia of childhood in Chinese patientsXiaoling Yang, Hua Gao, Jie Zhang, et al.Brain & Development|March 28, 2015
Founder mutation causes classical Fukuyama congenital muscular dystrophy (FCMD) in Chinese patientsHaipo Yang, Kazuhiro Kobayashi, Shuo Wang, et al.Pageof 12