Pei-Shan Wang

Clinical feature difference between juvenile amyotrophic lateral sclerosis with SPTLC1 and FUS mutations

Qiao Wei, Hong-Fu Li, Zhi-Ying Wu, 2023, Chinese medical journal.

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

Qiao Wei, Hong-Fu Li, Hai-Lin Dong, 2022, Molecular genetics & genomic medicine.

Biallelic variants in the COQ4 gene caused hereditary spastic paraplegia predominant phenotype.

Qiao Wei, Hong-Fu Li, Hai-Lin Dong, 2023, CNS neuroscience & therapeutics.