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Cardiocerebral channelopathy caused by KCND3 mutation in a child: A case report
Early repolarization syndrome is rare in children. Mutation of genes encoding ion channels could display mixed electrophysiological phenotype of Kv4.3 including both cardiac phenotype (early repolarization syndrome, atrial fibrillation) and cerebral phenotype (epilepsy, intellectual disability). Thi...
Autores principales: | Zhang, Yi, Jiang, He, Li, Xiao-mei |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9742191/ https://www.ncbi.nlm.nih.gov/pubmed/36518774 http://dx.doi.org/10.3389/fped.2022.1019122 |
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