Associated Papers
Neurodevelopmental Implications Underpinning Hereditary Spastic Paraplegia.
Zhi Y et al.
Cns Neuroscience & Therapeutics, 2025
39932116 (PubMed )
Supplement: CNS-31-e70260-s001.xlsx › SPG15
The genetic and phenotypic spectra of adult genetic leukoencephalopathies in a cohort of 309 patients.
Wu C et al.
Brain : a Journal of Neurology, 2023
36380532 (PubMed )
Supplement: awac426_supplementary_data.pdf
Case report: Hereditary spastic paraplegia with a novel homozygous mutation in ZFYVE26.
Lai ZH et al.
Frontiers in Neurology, 2023
37681008 (PubMed )
Supplement: Data_Sheet_1.xlsx › Sheet1
Genetic, clinical and neuroimaging profiles of sporadic and autosomal recessive hereditary spastic paraplegia cases in Chinese.
Dong Y et al.
Neuroscience Letters, 2021
A case of spastic paraplegia-15 with a novel pathogenic variant in ZFYVE26 gene.
Özdemir TR et al.
The International Journal of Neuroscience, 2019
Spastizin mutation in hereditary spastic paraplegia with thin corpus callosum.
Chakrabarty S et al.
Journal of Neurology, 2016
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