Associated Papers
Neurodevelopmental Implications Underpinning Hereditary Spastic Paraplegia.
Zhi Y et al.
Cns Neuroscience & Therapeutics, 2025
39932116 (PubMed )
Supplement: CNS-31-e70260-s001.xlsx › SPG2
A splicing mutation of proteolipid protein 1 in Pelizaeus-Merzbacher disease.
Omata T et al.
Brain & Development, 2016
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