Associated Papers
Neurodevelopmental Implications Underpinning Hereditary Spastic Paraplegia.
Zhi Y et al.
Cns Neuroscience & Therapeutics, 2025
39932116 (PubMed )
Supplement: CNS-31-e70260-s001.xlsx › SPG4
Valproate Treatment in an ALS Patient Carrying a c.194G>A Spastin Mutation and SMN2 Homozygous Deletion.
Tremolizzo L et al.
Case Reports in Neurological Medicine, 2014
Early-onset ALS with long-term survival associated with spastin gene mutation.
Meyer T et al.
Neurology, 2005
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