A rare CACNA1H variant associated with amyotrophic lateral sclerosis causes complete loss of Ca(v)3.2 T-type channel activity
一种与肌萎缩侧索硬化症相关的罕见 CACNA1H 变异会导致 Ca(v)3.2 T 型通道活性完全丧失
期刊:Molecular Brain
影响因子:2.9
doi:10.1186/s13041-020-00577-6
Stringer, Robin N; Jurkovicova-Tarabova, Bohumila; Huang, Sun; Haji-Ghassemi, Omid; Idoux, Romane; Liashenko, Anna; Souza, Ivana A; Rzhepetskyy, Yuriy; Lacinova, Lubica; Van Petegem, Filip; Zamponi, Gerald W; Pamphlett, Roger; Weiss, Norbert