Genotype-phenotype correlations of amyotrophic lateral sclerosis

by Li, Hong-Fu, Wu, Zhi-Ying
Published 2016

Identification of novel senataxin mutations in Chinese patients with autosomal recessive cerebellar ataxias by targeted next-generation sequencing

by Lu, Cong, Zheng, Yi-Cen, Dong, Yi, Li, Hong-Fu
Published 2016

FTL mutation in a Chinese pedigree with neuroferritinopathy

by Ni, Wang, Li, Hong-Fu, Zheng, Yi-Cen, Wu, Zhi-Ying
Published 2016

Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia Patients

by Wang, Hong-Xia, Li, Hong-Fu, Liu, Gong-Lu, Wen, Xiao-Dan, Wu, Zhi-Ying
Published 2016

Improving molecular diagnosis of Chinese patients with Charcot-Marie-Tooth by targeted next-generation sequencing and functional analysis

by Li, Li-Xi, Zhao, Shao-Yun, Liu, Zhi-Jun, Ni, Wang, Li, Hong-Fu, Xiao, Bao-Guo, Wu, Zhi-Ying
Published 2016

Urine-derived induced pluripotent stem cells as a modeling tool for paroxysmal kinesigenic dyskinesia

by Zhang, Shu-Zhen, Li, Hong-Fu, Ma, Li-Xiang, Qian, Wen-Jing, Wang, Zhong-Feng, Wu, Zhi-Ying
Published 2015

Modeling Neurological Disease by Rapid Conversion of Human Urine Cells into Functional Neurons

by Zhang, Shu-Zhen, Ma, Li-Xiang, Qian, Wen-Jing, Li, Hong-Fu, Wang, Zhong-Feng, Wang, Hong-Xia, Wu, Zhi-Ying
Published 2016