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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 6, 2002
[Case-control study and transmission/disequilibrium test of childhood absence epilepsy]Jianjun Lu, Yucai Chen, Yuehua Zhang, et al.Neuroscience Letters|May 29, 2003
The gene encoding GABBR1 is not associated with childhood absence epilepsy in the Chinese Han populationJianjun Lu, Yucai Chen, Hong Pan, et al.Journal of Human Genetics|January 23, 2009
Identification of novel EIF2B mutations in Chinese patients with vanishing white matter diseaseYe Wu, Yanxia Pan, Li Du, et al.Brain & Development|December 11, 2014
Identification and functional study of novel PLP1 mutations in Chinese patients with Pelizaeus-Merzbacher diseaseHan Xie, Hongchun Feng, Jinhua Ji, et al.BMC Medical Genetics|February 26, 2014
Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patientsYing Zhao, Xiaoying Zhang, Xinhua Bao, et al.Plos One|March 12, 2015
Fifteen novel EIF2B1-5 mutations identified in Chinese children with leukoencephalopathy with vanishing white matter and a long term follow-upHaihua Zhang, Lifang Dai, Na Chen, et al.Plos One|March 15, 2012
Functional studies of MLC1 mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cystsHan Xie, Jingmin Wang, Ajit Singh Dhaunchak, et al.Journal of Human Genetics|February 11, 2011
Functional analysis of recently identified mutations in eukaryotic translation initiation factor 2Bɛ (eIF2Bɛ) identified in Chinese patients with vanishing white matter diseaseXuerong Leng, Ye Wu, Xuemin Wang, et al.Molecular Genetics and Genomics : MGG|May 22, 2013
Novel POMGnT1 mutations cause muscle-eye-brain disease in Chinese patientsHui Jiao, Hiroshi Manya, Shuo Wang, et al.Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|January 14, 2016
[ATP1A3 gene mutations in patients with alternating hemiplegia of childhood]Xiaoling Yang, Yuehua Zhang, Dawei Yuan, et al.Pageof 12