Spinocerebellar ataxia type 2 (SCA2) with white matter involvement
- 24 June 2005
- journal article
- case report
- Published by Elsevier in Neuroscience Letters
- Vol. 381 (3) , 247-251
- https://doi.org/10.1016/j.neulet.2005.02.063
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Severe Cerebral White Matter Involvement in a Case of Dentatorubropallidoluysian Atrophy Studied at AutopsyArchives of Neurology, 2004
- Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two casesBrain, 2002
- CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphismsHuman Molecular Genetics, 2001
- Spinocerebellar ataxia 2 (SCA2): morphometric analyses in 11 autopsiesActa Neuropathologica, 1999
- Genes involved in hereditary ataxiasTrends in Neurosciences, 1998
- Molecular and Clinical Correlations in Spinocerebellar Ataxia 2: A Study of 32 FamiliesHuman Molecular Genetics, 1997
- Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeatsNature Genetics, 1996
- Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECTNature Genetics, 1996
- Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2Nature Genetics, 1996
- Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23–q24.1Genomics, 1995