Effects of mutant huntingtin inactivation on Huntington disease-related behaviours in the BACHD mouse model.
Rachel Y CheongBarbara BaldoMuhammad U SajjadDeniz KirikÅsa PetersénPublished in: Neuropathology and applied neurobiology (2021)
Our results indicate that widespread targeting and the timing of interventions aimed at reducing mutant HTT are important factors to consider when developing disease-modifying therapies for HD.