Genetic heterogeneity in inherited spastic paraplegia associated with epilepsy
- 13 January 2003
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 117A (2) , 116-121
- https://doi.org/10.1002/ajmg.a.10141
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- A refined physical and transcriptional map of the SPG9 locus on 10q23.3–q24.2European Journal of Human Genetics, 2000
- A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-q34American Journal of Human Genetics, 2000
- Novel Locus for Autosomal Dominant Hereditary Spastic Paraplegia, on Chromosome 8qAmerican Journal of Human Genetics, 1999
- Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p.Journal of Medical Genetics, 1998
- Localization of a gene for partial epilepsy to chromosome 10qNature Genetics, 1995
- The 1993–94 Généthon human genetic linkage mapNature Genetics, 1994
- Hereditary Spastic ParaplegiasSeminars in Neurology, 1993
- Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14qNature Genetics, 1993
- Spastic paraplegia, epilepsy, and mental retardation in several members of a family: A novel genetic disorderAmerican Journal of Medical Genetics, 1993
- Strategies for multilocus linkage analysis in humans.Proceedings of the National Academy of Sciences, 1984