Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome-Reference-Cited by-同舟云学术

Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome

Published:2008-04 Issue:4 Volume:82 Page:992-1002
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

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

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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4. Prevalence of hereditary ataxias and spastic paraplegias in Molise, a region of Italy;Filla;J. Neurol.,1992

5. Strumpell's familial spastic paraplegia: genetics and neuropathology;Behan;J. Neurol. Neurosurg. Psychiatry,1974

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