Identification of theSPG15Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome


Sylvain Hanein,Elodie Martin,Amir Boukhris,Paula Byrne,Cyril Goizet,Abdelmadjid Hamri,Ali Benomar,Alexander Lossos,Paola Denora,José Fernandez,Nizar Elleuch,Sylvie Forlani,Alexandra Durr,Imed Feki,Michael Hutchinson,Filippo M. Santorelli, et al.


The American Journal of Human Genetics




11 April 2008

Copyright © 2008, Elsevier

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