Somatic expansion of the (CAG) n repeat in Huntington disease brains
- 1 March 1995
- journal article
- Published by Springer Nature in Human Genetics
- Vol. 95 (3) , 270-274
- https://doi.org/10.1007/bf00225192
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA)Nature Genetics, 1994
- Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12pNature Genetics, 1994
- Dynamic mutation in Dutch Huntington's disease patients: increased paternal repeat instability extending to within the normal size range.Journal of Medical Genetics, 1993
- Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissuesNature Genetics, 1993
- Differential 3′ polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expressionHuman Molecular Genetics, 1993
- Effect of the myotonic dystrophy (DM) mutation on mRNA levels of the DM geneNature Genetics, 1993
- A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomesMolecular and Cellular Probes, 1993
- Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family memberPublished by Elsevier ,1992
- Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophyNature, 1991
- A simple salting out procedure for extracting DNA from human nucleated cellsNucleic Acids Research, 1988