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!
What will I do when I need that information? Please tell me, Jake, so I don't have to do the leg work.
Found it through various medical journals - I can't remember the exact names but it's out there if you search hard enough.
I could answer most questions you have - without citation of course. If there is anything you need to know, just message me.
