DNA trinucleotide repeat expansions are known to be associated with several hereditary neurodegenerative disorders, including Huntington disease, Fragile X syndrome and spinocerebellar ataxia.

Huntington'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 ...