To derive the iPSC lines, we retrovirally introduced the four reprogramming factors (Oct3/4, Sox2, c-MYC and Klf4) [26,27] into dermal fibroblasts harvested from a male patient with adult onset HD (50 CAG repeats), his daughter with juvenile-HD (109 CAG repeats) and non-related neonatal foreskin fibroblasts (28 CAG repeats) as controls. Here, SOX2 is linked to Huntington disease.