I've been spending the last 5-6 weeks studying CAG related disorders, namely Huntington's Disease. I've had a nagging question that I couldn't seem to find the answer to, and that question is: "What is the genomic component that is universal among all CAG-repeat disorders?" We know that they are dominantly inherited, and each offspring has a 50/50 chance to receive Huntington's Disease but what is the actual 'cause' of the disease? What makes these repetitions inheritable? Any and all insight is helpful into developing my knowledge. Thanks!