Spastic paraplegia as the predominant phenotype in a cohort of Chinese patients with adrenoleukodystrophy

por Luo, Wen‐Jiao, Wei, Qiao, Dong, Hai‐Lin, Yan, Yang‐Tian, Chen, Mei‐Jiao, Li, Hong‐Fu
Publicado 2019

A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia

por Wei, Qiao, Wang, Pei‐Shan, Dong, Hai‐Lin, Luo, Wen‐Jiao, Wu, Zhi‐Ying, Li, Hong‐Fu
Publicado 2022

Identified novel heterozygous HTRA1 pathogenic variants in Chinese patients with HTRA1-associated dominant cerebral small vessel disease

por Chen, Mei-Jiao, Zhang, Yi, Luo, Wen-Jiao, Dong, Hai-Lin, Wei, Qiao, Zhang, Juan, Ruan, Qi-Qi, Ni, Wang, Li, Hong-Fu
Publicado 2022

TMEM151A variants cause paroxysmal kinesigenic dyskinesia

por Li, Hong-Fu, Chen, Yu-Lan, Zhuang, Ling, Chen, Dian-Fu, Ke, Hua-Zhen, Luo, Wen-Jiao, Liu, Gong-Lu, Wu, Sheng-Nan, Zhou, Wen-Hao, Xiong, Zhi-Qi, Wu, Zhi-Ying
Publicado 2021

Author Correction: TMEM151A variants cause paroxysmal kinesigenic dyskinesia

por Li, Hong-Fu, Chen, Yu-Lan, Zhuang, Ling, Chen, Dian-Fu, Ke, Hua-Zhen, Luo, Wen-Jiao, Liu, Gong-Lu, Wu, Sheng-Nan, Zhou, Wen-Hao, Xiong, Zhi-Qi, Wu, Zhi-Ying
Publicado 2021