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• W2025849896 endingPage "1704" @default.
• W2025849896 startingPage "1698" @default.
• W2025849896 abstract "Trinucleotide repeat expansions have been identified as the underlying mutation in an increasing number of human genetic diseases, such as fragile site syndromes, myotonic dystrophy and several neurodegenerative disorders including Huntington's disease. By an unknown mechanism, polymorphic GC-rich triplet repeats expand in all these diseases. The expansions of a CCG repeat in fragile-site-associated disorders and the CTG repeat (in the 3'-untranslated region of the myotonin kinase gene) causing myotonic dystrophy are very large, whereas small expansions of CAG repeats have been identified in the open reading frame of genes in a number of neurological genetic disorders." @default.
• W2025849896 created "2016-06-24" @default.
• W2025849896 creator A5007073262 @default.
• W2025849896 creator A5019720850 @default.
• W2025849896 date "1995-01-01" @default.
• W2025849896 modified "2023-09-23" @default.
• W2025849896 title "Trinucleotide repeat expansion and human disease" @default.
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• W2025849896 doi "https://doi.org/10.1002/elps.11501601282" @default.
• W2025849896 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/8582359" @default.
• W2025849896 hasPublicationYear "1995" @default.
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