Unstable trinucleotide repeats and the diagnosis of neurodegenerative disease
- 1 June 1994
- journal article
- Published by Elsevier BV in Human Pathology
- Vol. 25 (6), 598-601
- https://doi.org/10.1016/0046-8177(94)90226-7
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1Nature Genetics, 1993
- An expanding enigmaCurrent Biology, 1993
- A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomesCell, 1993
- Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisNature, 1993
- Framing β–amyloidNature Genetics, 1992
- An Unstable Triplet Repeat in a Gene Related to Myotonic Muscular DystrophyScience, 1992
- Myotonic Dystrophy Mutation: an Unstable CTG Repeat in the 3′ Untranslated region of the GeneScience, 1992
- Molecular basis of myotonic dystrophy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family memberCell, 1992
- Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophyNature, 1991
- Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromeCell, 1991