DNA trinucleotide repeat expansions are known to be associated with several hereditary neurodegenerative disorders, including Huntington disease, Fragile X syndrome and spinocerebellar ataxia.
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Brain Changes Emerge Decades Before Huntington's DiagnosisHuntington's is an autosomal dominant genetic disorder caused by extended CAG trinucleotide repeats in the huntingtin (HTT) gene. The sequence tends to expand continually in a process known as ...
Cure Rare Disease (CRD) announced it has been awarded a $5.69 million grant from the California Institute for Regenerative ...
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