Intrinsic mutant HTT-mediated defects in oligodendroglia cause myelination deficits and behavioral abnormalities in Huntington disease
少突胶质细胞内在突变 HTT 介导的缺陷导致亨廷顿病的髓鞘形成缺陷和行为异常
期刊:Proceedings of the National Academy of Sciences of the United States of America
影响因子:
doi:10.1073/pnas.1818042116
Costanza Ferrari Bardile, Marta Garcia-Miralles, Nicholas S Caron, Nirmala Arul Rayan, Sarah R Langley, Nathan Harmston, Ana Maria Rondelli, Roy Tang Yi Teo, Sabine Waltl, Lisa M Anderson, Han-Gyu Bae, Sangyong Jung, Anna Williams, Shyam Prabhakar, Enrico Petretto, Michael R Hayden, Mahmoud A Poulad