Mouse models of triplet repeat diseases.

doi:10.1385/MB:32:2:147

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Article

Mouse models of triplet repeat diseases.

Molecular biotechnology - 1 Feb 2006

Bates Gillian P, Gonitel Roman

Abstract excerpt

Triplet repeat expansions were first discovered in 1991 and since then have been found to be the mutation underlying a range of neurodegenerative, neuromuscular, and cognitive disorders including fragile X syndrome, myotonic dystrophy, Friedreich's ataxia, and the polyglutamine disorders that include Huntington's disease. The repeats exert their detrimental effects through different molecular mechanisms dependent...

Topics

Animals
Disease Models, Animal
Genetic Diseases, Inborn
Humans
Mice
Molecular Biology
Mutation
Trinucleotide Repeats

Source

Open in PubMed

Identifiers

PMID: 16444016
DOI: 10.1385/MB:32:2:147

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