Molecular Mechanisms of Epileptic Encephalopathy Caused by KCNMA1 Loss-of-Function Mutations

The gene kcnma1 encodes the α-subunit of high-conductance calcium- and voltage-dependent K(+) (BK) potassium channel. With the development of generation gene sequencing technology, many KCNMA1 mutants have been identified and are more closely related to generalized epilepsy and paroxysmal dyskinesia...

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Detalles Bibliográficos
Autores principales: Yao, Yu, Qu, Dongxiao, Jing, Xiaoping, Jia, Yuxiang, Zhong, Qi, Zhuo, Limin, Chen, Xingxing, Li, Guoyi, Tang, Lele, Zhu, Yudan, Zhang, Xuemei, Ji, Yonghua, Li, Zhiping, Tao, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pharmacology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793784/
https://www.ncbi.nlm.nih.gov/pubmed/35095492
http://dx.doi.org/10.3389/fphar.2021.775328

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793784/
https://www.ncbi.nlm.nih.gov/pubmed/35095492
http://dx.doi.org/10.3389/fphar.2021.775328

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