Identification of genetic variants in a pedigree associated with epilepsy by using whole exome sequencing and whole genome sequencing

by Qin-Qin Zhang, Zi-Hua Wang, Jun-Shi Zhang, Jun-Nan Guo, Xu-Hong Lin, Lei An
Published 2021-06-01

Linking cortical astrocytic neogenin deficiency to the development of Moyamoya disease–like vasculopathy

by Xiao Ren, Ling-Ling Yao, Jin-Xiu Pan, Jun-Shi Zhang, Lin Mei, Yong-Gang Wang, Wen-Cheng Xiong
Published 2021-07-01