Identification of the SPG15 gene, encoding spastizin, as a frequent cause of complicated autosomal-recessive spastic paraplegia, including Kjellin syndrome.
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A. Durr | M. Hutchinson | S. Hanein | S. Forlani | N. Elleuch | A. Brice | G. Stevanin | F. Santorelli | P. Byrne | C. Goizet | A. Boukhris | I. Feki | C. Mhiri | E. Martin | P. Denora | J. Fernandez | A. Benomar | A. Lossos | A. Hamri