How can we define the information content of the mutation responsible for Huntington’s Disease? It occurs in a non-coding section, it’s technically a collection of similiar mutations, and it seems to have something to do with the physical structure of the chromosome rather than coding in the simple sense.
How can we define the information content of the mutation responsible for Huntington’s Disease? It occurs in a non-coding section, it’s technically a collection of similiar mutations, and it seems to have something to do with the physical structure of the chromosome rather than coding in the simple sense.