Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia-Reference-Cited by-同舟云学术

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

Published:1999-11 Issue:3 Volume:23 Page:296-303
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Hazan Jamilé,Fonknechten Nùria,Mavel Delphine,Paternotte Caroline,Samson Delphine,Artiguenave François,Davoine Claire-Sophie,Cruaud Corinne,Dürr Alexandra,Wincker Patrick,Brottier Philippe,Cattolico Laurence,Barbe Valérie,Burgunder Jean-Marc,Prud'homme Jean-François,Brice Alexis,Fontaine Bertrand,Heilig Roland,Weissenbach Jean

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1199_296.pdf

Reference48 articles.

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

3. Werderlin, L. Hereditary ataxias. Occurence and clinical features. Acta Neurol. Scand. 73 (suppl. 106), 124 (1986).

4. Skre, H. Hereditary spastic paraplegia in western Norway. Clin. Genet. 6, 165–183 (1974).

5. Hazan, J. et al. Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q. Nature Genet. 5, 163–167 (1993).

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