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SPG11compound mutations in spastic paraparesis with thin corpus callosum
- Source :
- Neurology (Ovid); July 2008, Vol. 71 Issue: 5 p332-336, 5p
- Publication Year :
- 2008
-
Abstract
- Autosomal recessive hereditary spastic paraparesis with thin corpus callosum (ARHSP-TCC) is being increasingly recognized as a variety of spastic paraplegia with mental retardation. SPG11gene mutations have been reported to be associated with ARHSP-TCC.
Details
- Language :
- English
- ISSN :
- 00283878 and 1526632X
- Volume :
- 71
- Issue :
- 5
- Database :
- Supplemental Index
- Journal :
- Neurology (Ovid)
- Publication Type :
- Periodical
- Accession number :
- ejs49021053
- Full Text :
- https://doi.org/10.1212/01.wnl.0000319646.23052.d1