Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners-Reference-Cited by-同舟云学术

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Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners

Published:2005-12-08 Issue:2 Volume:15 Page:307-318
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Sanderson Christopher M.,Connell James W.,Edwards Thomas L.,Bright Nicholas A.,Duley Simon,Thompson Amanda,Luzio J. Paul,Reid Evan

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/15/2/307/1620198/ddi447.pdf

Reference42 articles.

1. Harding, A.E.(1984) The Hereditary Ataxias and Related Disorders. Churchill Livingstone, Edinburgh.

2. Fink, J.K. (2002) Hereditary spastic paraplegia. In Rimoin, D.L., Pyeritz, R.E., Connor, J.M. and Korf, B.R. (eds.), Emory and Rimoin's Principles and Practice of Medical Genetics, 4th edn. Harcoart, London, UK, pp. 3124–3145.

3. Reid, E. (2003) Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias. J. Med. Genet., 40, 35–39.

4. Polo, J.M., Calleja, J., Combarros, O. and Berciano, J. (1991) Hereditary ataxias and paraplegias in Cantabria, Spain. An epidemiological and clinical study. Brain, 114, 855–866.

5. Fink, J.K. (2003) The hereditary spastic paraplegias: nine genes and counting. Arch. Neurol., 60, 1045–1049.

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