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  • Molecular assay reagents intended to identify the number of copies of a sequence of three-letter words known as trinucleotide repeats in a gene\'s DNA. A variation from the normal number of trinucleotide repeat copies may produce altered DNA and improper gene functioning, resulting in full mutation. Mutations in specific genes are related to one or more particular diseases, including spinocerebellar ataxia, fragile X syndrome, and Friedreich\'s ataxia.
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