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Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration file Files in this Data Supplement:
Brain Stevanin et al.
131: 772
Supplementary Data
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Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration file Files in this Data Supplement:
Brain Stevanin et al.
131: 772
Supplementary Data
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