Asymptomatic CTG expansion at the SCA8 locus is associated with cerebellar atrophy on MRI
- 1 December 2000
- journal article
- case report
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 182 (1) , 76-79
- https://doi.org/10.1016/s0022-510x(00)00446-9
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- High Germinal Instability of the (CTG)n at the SCA8 Locus of Both Expanded and Normal AllelesAmerican Journal of Human Genetics, 2000
- An Unstable Trinucleotide-Repeat Region on Chromosome 13 Implicated in Spinocerebellar Ataxia: A Common Expansion LocusAmerican Journal of Human Genetics, 2000
- Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxiaNature Genetics, 2000
- Are (CTG)n expansions at the SCA8 locus rare polymorphisms?Nature Genetics, 2000
- Molecular and clinical analyses of spinocerebellar ataxia type 8 in JapanNeurology, 2000
- An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)Nature Genetics, 1999
- Molecular analysis of a de novo mutation for spinocerebellar ataxia type 6 and (CAG)n repeat units in normal elder controlsJournal of the Neurological Sciences, 1998
- Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effectsNature Genetics, 1993