Intrinsic mutant HTT-mediated defects in oligodendroglia cause myelination deficits and behavioral abnormalities in Huntington disease

Autor:	Bardile, Costanza Ferrari, Garcia-Miralles, Marta, Caron, Nicholas S., Rayan, Nirmala Arul, Langley, Sarah R., Harmston, Nathan, Rondelli, Ana Maria, Teo, Roy Tang Yi, Waltl, Sabine, Anderson, Lisa M., Bae, Han-Gyu, Jung, Sangyong, Williams, Anna, Prabhakar, Shyam, Petretto, Enrico, Hayden, Michael R., Pouladi, Mahmoud A.
Zdroj:	Proceedings of the National Academy of Sciences of the United States of America, 2019 May 01. 116(19), 9622-9627.
Databáze:	JSTOR Journals
Externí odkaz:	https://www.jstor.org/stable/26705153 Zobrazit plný text záznamu