Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10

Volume: 30, Issue: 2
Published: Feb 1, 2009
Abstract
Hereditary spastic paraplegias (HSP) constitute a heterogeneous group of neurodegenerative disorders characterized by slowly progressive spasticity of the lower extremities. Only a few different mutations in the SPG10 gene, KIF5A, have been described in pure dominant forms of the disease. We sequenced the motor domain of KIF5A in a large panel of 205 European HSP patients with either pure or complicated forms of the disease. We identified eight...
Paper Details
Title
Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10
Published Date
Feb 1, 2009
Volume
30
Issue
2
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