DOI:
10.1055/s-00000071
Seminars in Neurology
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References
Stevanin G, Santorelli FM, Azzedine H , et al.
Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum.
Nat Genet 2007;
39 (3) 366-372
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