The Significance of LINE-1 in Huntington Disease
Wahibah Hannan Huntington Disease (HD) is an autosomal dominant neurodegenerative disorder characterized by progressive motor impairment, psychiatric disturbances, and cognitive decline1. HD is caused by an expansion of a CAG trinucleotide repeat in the huntingtin gene. The mutant huntingtin protein gains toxic function and results in neurodegeneration, specifically in the…