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
Neurodevelopmental Implications Underpinning Hereditary Spastic Paraplegia.
Zhi Y et al.
Cns Neuroscience & Therapeutics, 2025
39932116 (PubMed )
Supplement: CNS-31-e70260-s001.xlsx › SPG4
Hereditary spastic paraplegia due to SPAST mutations in 151 Dutch patients: new clinical aspects and 27 novel mutations.
de Bot ST et al.
Journal of Neurology, Neurosurgery, and Psychiatry, 2010
Select a paper to view details