Role of Bβ1 overexpression in the pathogenesis of SCA12.
Chengqian ZhouFan TangTao DongHans B LiuLeon DengRussell L MargolisPan P LiPublished in: Movement disorders : official journal of the Movement Disorder Society (2024)
The SCA12 mutation leads to overexpression of PPP2R2B Bβ1 and to expression of a protein containing a long polyserine tract; both these effects potentially contribute to SCA12 pathogenesis. © 2024 International Parkinson and Movement Disorder Society.