Associated Papers
Neurodevelopmental Implications Underpinning Hereditary Spastic Paraplegia.
Zhi Y et al.
Cns Neuroscience & Therapeutics, 2025
39932116 (PubMed )
Supplement: CNS-31-e70260-s001.xlsx › SPG1
Novel mutations in the L1CAM gene support the complexity of L1 syndrome.
Bertolin C et al.
Journal of the Neurological Sciences, 2010
A novel missense mutation in the L1CAM gene in a boy with L1 disease.
Simonati A et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2006
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