Associated Papers
A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia.
Wei Q et al.
Molecular Genetics & Genomic Medicine, 2022
Novel Frameshift Heterozygous Mutation in UBAP1 Gene Causing Spastic Paraplegia-80: Case Report With Literature Review.
Zhang C et al.
Frontiers in Neurology, 2022
A novel mutation in the UBAP1 gene causing hereditary spastic paraplegia: A case report and overview of the genotype-phenotype correlation.
Li P et al.
Frontiers in Genetics, 2022
Select a paper to view details