Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum-Reference-Cited by-同舟云学术

Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum

Published:2007-02-18 Issue:3 Volume:39 Page:366-372
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Stevanin Giovanni,Santorelli Filippo M,Azzedine Hamid,Coutinho Paula,Chomilier Jacques,Denora Paola S,Martin Elodie,Ouvrard-Hernandez Anne-Marie,Tessa Alessandra,Bouslam Naïma,Lossos Alexander,Charles Perrine,Loureiro José L,Elleuch Nizar,Confavreux Christian,Cruz Vítor T,Ruberg Merle,Leguern Eric,Grid Djamel,Tazir Meriem,Fontaine Bertrand,Filla Alessandro,Bertini Enrico,Durr Alexandra,Brice Alexis

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1980.pdf

Reference24 articles.

1. Harding, A.E. Classification of the hereditary ataxias and paraplegias. Lancet 1, 1151–1155 (1983).

2. Nakamura, A. et al. Familial spastic paraplegia with mental impairment and thin corpus callosum. J. Neurol. Sci. 131, 35–42 (1995).

3. Winner, B. et al. Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11). Arch. Neurol. 61, 117–121 (2004).

4. Martinez, M.F. et al. Genetic localization of a new locus for recessive familial spastic paraparesis to 15q13–15. Neurology 53, 50–56 (1999).

5. Casali, C. et al. Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum. Neurology 62, 262–268 (2004).

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