Associated Papers
Neurodevelopmental Implications Underpinning Hereditary Spastic Paraplegia.
Zhi Y et al.
Cns Neuroscience & Therapeutics, 2025
39932116 (PubMed )
Supplement: CNS-31-e70260-s001.xlsx › SPG12
RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity.
Maroofian R et al.
Brain : a Journal of Neurology, 2024
New phenotype of RTN2-related spectrum: Complicated form of spastic paraplegia-12.
Tian W et al.
Annals of Clinical and Translational Neurology, 2022
Mutations in the ER-shaping protein reticulon 2 cause the axon-degenerative disorder hereditary spastic paraplegia type 12.
Montenegro G et al.
The Journal of Clinical Investigation, 2012
Select a paper to view details