Associated Papers
Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia.
Zhu R et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2025
41312619 (PubMed )
Supplement: supplement_1.xlsx › Supplemental_Table_4
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
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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