Clinical and Genetic Heterogeneity in a Cohort of Chinese Children With Dopa-Responsive Dystonia

by Yan Chen, Xinhua Bao, Yongxin Wen, Jiaping Wang, Qingping Zhang, Jiayou Yan
Published 2020-02-01

Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation

by Jiaping Wang, Qingping Zhang, Yan Chen, Shujie Yu, Xiru Wu, Xinhua Bao, Yongxin Wen
Published 2018-10-01

CACNA1A Gene Variants in Eight Chinese Patients With a Wide Range of Phenotypes

by Linxia Zhang, Linxia Zhang, Yongxin Wen, Qingping Zhang, Yan Chen, Jiaping Wang, Kaili Shi, Lijun Du, Xinhua Bao
Published 2020-12-01

Report of the Largest Chinese Cohort With SLC19A3 Gene Defect and Literature Review

by Jiaping Wang, Junling Wang, Xiaodi Han, Zhimei Liu, Yanli Ma, Guohong Chen, Haoya Zhang, Dan Sun, Ruifeng Xu, Yi Liu, Yuqin Zhang, Yongxin Wen, Xinhua Bao, Qian Chen, Fang Fang
Published 2021-07-01