Opening the KV3.1 gates: A therapeutic strategy for progressive myoclonus epilepsy type 7?
CELL REPORTS MEDICINE(2024)
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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