Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy
离子通道病是与小脑萎缩相关的遗传性共济失调的常见病因
期刊:Movement Disorders Clinical Practice
影响因子:2.7
doi:10.1002/mdc3.13086
Gauquelin, Laurence; Hartley, Taila; Tarnopolsky, Mark; Dyment, David A; Brais, Bernard; Geraghty, Michael T; Tétreault, Martine; Ahmed, Sohnee; Rojas, Samantha; Choquet, Karine; Majewski, Jacek; Bernier, François; Innes, Allan Micheil; Rouleau, Guy; Suchowersky, Oksana; Boycott, Kym M; Yoon, Grace
