Cong-Xin Chen

Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia

Zhi-ying Wu, Qiao Wei, Hong-Fu Li, 2019, Translational Neurodegeneration.

Identification and functional characterization of novel GDAP1 variants in Chinese patients with Charcot–Marie–Tooth disease

Ge Bai, Hai-Lin Dong, Gonglu Liu, 2020, Annals of clinical and translational neurology.

Identification and functional analysis of novel mutations in the SOD1 gene in Chinese patients with amyotrophic lateral sclerosis

A. Gitler, Qiao Wei, Hong-Fu Li, 2019, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Genetic spectrum and clinical profiles in a southeast Chinese cohort of Charcot‐Marie‐Tooth disease

Qiao Wei, Huan Ma, Ge Bai, 2019, Clinical genetics.

Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia

Qiao Wei, Hong-Fu Li, Zhi-Jun Liu, 2019, Translational Neurodegeneration.

A novel WARS mutation causes distal hereditary motor neuropathy in a Chinese family.

Hai-Lin Dong, Cong-Xin Chen, Zhi-Ying Wu, 2019, Brain : a journal of neurology.