“…Dysfunctional RBPs, including hnRNP A1 and TAR-DNA binding protein , have been shown to contribute to neurological diseases including amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTLD), Alzheimer's disease (AD), and most recently, MS (Ash, Vanderweyde, Youmans, Apicco, & Wolozin, 2014;Deng, Gao, & Jankovic, 2014;Kabashi et al, 2008;Kim et al, 2013;Lagier-Tourenne, Polymenidou, & Cleveland, 2010;Maziuk et al, 2018;Salapa, Johnson, Hutchinson, Popescu, & Levin, 2018;Salapa, Lee, Shin, & Levin, 2017;Vanderweyde et al, 2012). Dysfunctional RBPs, including hnRNP A1 and TAR-DNA binding protein , have been shown to contribute to neurological diseases including amyotrophic lateral sclerosis (ALS), frontotemporal dementia (FTLD), Alzheimer's disease (AD), and most recently, MS (Ash, Vanderweyde, Youmans, Apicco, & Wolozin, 2014;Deng, Gao, & Jankovic, 2014;Kabashi et al, 2008;Kim et al, 2013;Lagier-Tourenne, Polymenidou, & Cleveland, 2010;Maziuk et al, 2018;Salapa, Johnson, Hutchinson, Popescu, & Levin, 2018;Salapa, Lee, Shin, & Levin, 2017;Vanderweyde et al, 2012).…”