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Clinical Genetics|January 11, 2011
Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutationsA Arnoldi, C Crimella, E Tenderini, et al.Clinical Genetics|June 1, 2011
Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2C Crimella, C Baschirotto, A Arnoldi, et al.Journal of Medical Genetics|February 7, 2009
Point mutations and a large intragenic deletion in SPG11 in complicated spastic paraplegia without thin corpus callosumC Crimella, A Arnoldi, F Crippa, et al.Pageof 3