Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia
- 21 May 2002
- journal article
- letter
- Published by Wiley in Annals of Neurology
- Vol. 51 (6), 794-795
- https://doi.org/10.1002/ana.10185
Abstract
No abstract availableKeywords
This publication has 3 references indexed in Scilit:
- Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegiaNature Genetics, 2001
- Structure of human guanylate-binding protein 1 representing a unique class of GTP-binding proteinsNature, 2000
- Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegiaNature Genetics, 1999