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
Evaluation of loss of function as an explanation for SPG4-based hereditary spastic paraplegia.
Solowska JM et al.
Human Molecular Genetics, 2010
Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia.
Sauter S et al.
Human Mutation, 2002
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