Opening the KV3.1 gates: A therapeutic strategy for progressive myoclonus epilepsy type 7?

被引：0
|
作者：
Gandini, Maria A. [1 ]
Zamponi, Gerald W. [1 ]
机构：
[1] Univ Calgary, Dept Clin Neurosci, Calgary, AB, Canada
来源：
CELL REPORTS MEDICINE | 2024年 / 5卷 / 02期
关键词：
ATAXIA;
D O I：
10.1016/j.xcrm.2024.101425
中图分类号：
Q2 [细胞生物学];
学科分类号：
071009 ; 090102 ;
摘要：
Progressive myoclonus epilepsy type 7, a debilitating neurological disorder, is caused by a loss -of -function mutation in the KV3.1 channel. Exciting work by Feng et al.1 utilizes a new knockin mouse model to identify a potential therapeutic intervention.
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页数：2
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