CACNA1A Mutations Associated With Epilepsies and Their Molecular Sub-Regional Implications

PurposePreviously, mutations in the voltage-gated calcium channel subunit alpha1 A (CACNA1A) gene have been reported to be associated with paroxysmal disorders, typically as episodic ataxia type 2. To determine the relationship between CACNA1A and epilepsies and the role of molecular sub-regional on...

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Detalhes bibliográficos
Main Authors: Xue-Lian Li, Zong-Jun Li, Xiao-Yu Liang, De-Tian Liu, Mi Jiang, Liang-Di Gao, Huan Li, Xue-Qing Tang, Yi-Wu Shi, Bing-Mei Li, Na He, Bin Li, Wen-Jun Bian, Yong-Hong Yi, Chuan-Fang Cheng, Jie Wang
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2022-05-01
Colecção:Frontiers in Molecular Neuroscience
Assuntos:
CACNA1A
partial epilepsy
childhood absence epilepsy
genotype-phenotype correlation
molecular sub-regional implication
Acesso em linha:https://www.frontiersin.org/articles/10.3389/fnmol.2022.860662/full
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