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 clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15.
Saffari A et al.
Brain : a Journal of Neurology, 2023
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
Novel c.C2254T (p.Q752*) mutation in ZFYVE26 (SPG15) gene in a patient with hereditary spastic paraparesis.
Vinci M et al.
Journal of Genetics, 2018
Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48.
Pensato V et al.
Brain : a Journal of Neurology, 2014
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