Incomplete penetrance in an SPG3A -linked family with a new mutation in the atlastin gene
- 8 June 2004
- journal article
- case report
- Published by Wolters Kluwer Health in Neurology
- Vol. 62 (11) , 2138-2139
- https://doi.org/10.1212/01.wnl.0000127698.88895.85
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- The Hereditary Spastic ParaplegiasArchives of Neurology, 2003
- SPG3ANeurology, 2002
- Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegiaNature Genetics, 2001
- A Functional Link between Dynamin and the Actin Cytoskeleton at PodosomesThe Journal of cell biology, 2000