Functional Genomic Analyses of Mendelian and Sporadic Disease Identify Impaired eIF2α Signaling as a Generalizable Mechanism for Dystonia
孟德尔遗传病和散发性疾病的功能基因组学分析表明，eIF2α信号通路受损是肌张力障碍的普遍机制。
期刊:Neuron
影响因子:15
doi:10.1016/j.neuron.2016.11.012
Rittiner, Joseph E; Caffall, Zachary F; Hernández-Martinez, Ricardo; Sanderson, Sydney M; Pearson, James L; Tsukayama, Kaylin K; Liu, Anna Y; Xiao, Changrui; Tracy, Samantha; Shipman, Miranda K; Hickey, Patrick; Johnson, Julia; Scott, Burton; Stacy, Mark; Saunders-Pullman, Rachel; Bressman, Susan; Simonyan, Kristina; Sharma, Nutan; Ozelius, Laurie J; Cirulli, Elizabeth T; Calakos, Nicole
