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Authors: Vitor T. Cruz
Journal Article
Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration Get access
in
Brain
Brain, Volume 131, Issue 3, March 2008, Pages 772–784, https://doi.org/10.1093/brain/awm293
Published: 13 December 2007
