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pro vyhledávání: '"Bethany Fitsimmons"'
Autor:
Amber L. Southwell, Hailey Findlay-Black, Yuanyun Xie, Bethany Fitsimmons, Michael E. Østergaard, C. Frank Bennett, Niels H. Skotte, Louisa Dal Cengio, Punit P. Seth, Crystal N. Doty, Michael R. Hayden, Erika B. Villanueva, Douglas R. Langbehn, Lynn A. Raymond, Lisa M. Anderson, Holly B. Kordasiewicz, Eric E. Swayze, Matthew P. Parsons, Nicholas S. Caron
Publikováno v:
Science Translational Medicine. 10
Huntington disease (HD) is an autosomal dominant neurodegenerative disorder caused by a mutation in the huntingtin (HTT) protein, resulting in acquisition of toxic functions. Previous studies have shown that lowering mutant HTT has the potential to b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7234a2400b48305341d35ff493f065e4
https://doi.org/10.1126/scitranslmed.aar3959
https://doi.org/10.1126/scitranslmed.aar3959
