Pathomechanisms of a CLCN1 Mutation Found in a Russian Family Suffering From Becker's Myotonia
俄罗斯贝克尔氏肌强直患者家族中发现 CLCN1 突变的发病机制
期刊:Frontiers in Neurology
影响因子:2.7
doi:10.3389/fneur.2020.01019
Concetta Altamura, Evgeniya A Ivanova, Paola Imbrici, Elena Conte, Giulia Maria Camerino, Elena L Dadali, Alexander V Polyakov, Sergei Aleksandrovich Kurbatov, Francesco Girolamo, Maria Rosaria Carratù, Jean-François Desaphy
