Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene.
The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1...
Main Authors: | , , , , , , , |
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Format: | Journal article |
Language: | English |
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1994
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author | Hummerich, H Baxendale, S Mott, R Kirby, S MacDonald, M Gusella, J Lehrach, H Bates, G |
author_facet | Hummerich, H Baxendale, S Mott, R Kirby, S MacDonald, M Gusella, J Lehrach, H Bates, G |
author_sort | Hummerich, H |
collection | OXFORD |
description | The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases. We report here the identification of all ten classes of trinucleotide repeats within a 2 Mbp region of 4p16.3 containing the Huntington's disease (HD) gene. Fifty one triplet repeats were identified and localised on a high resolution restriction map of a cosmid contig covering this region. This included the triplet repeat (CAG)n, which has subsequently been shown to be expanded in Huntington's disease patients. |
first_indexed | 2024-03-07T00:23:43Z |
format | Journal article |
id | oxford-uuid:7d67d769-a6e4-4514-bacd-6bcad7c3640b |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-07T00:23:43Z |
publishDate | 1994 |
record_format | dspace |
spelling | oxford-uuid:7d67d769-a6e4-4514-bacd-6bcad7c3640b2022-03-26T21:03:28ZDistribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:7d67d769-a6e4-4514-bacd-6bcad7c3640bEnglishSymplectic Elements at Oxford1994Hummerich, HBaxendale, SMott, RKirby, SMacDonald, MGusella, JLehrach, HBates, GThe recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will lead to interest in the identification of such sequences in regions related to other diseases. We report here the identification of all ten classes of trinucleotide repeats within a 2 Mbp region of 4p16.3 containing the Huntington's disease (HD) gene. Fifty one triplet repeats were identified and localised on a high resolution restriction map of a cosmid contig covering this region. This included the triplet repeat (CAG)n, which has subsequently been shown to be expanded in Huntington's disease patients. |
spellingShingle | Hummerich, H Baxendale, S Mott, R Kirby, S MacDonald, M Gusella, J Lehrach, H Bates, G Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene. |
title | Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene. |
title_full | Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene. |
title_fullStr | Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene. |
title_full_unstemmed | Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene. |
title_short | Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene. |
title_sort | distribution of trinucleotide repeat sequences across a 2 mbp region containing the huntington s disease gene |
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