Genetic and clinical analysis of children with early-onset epilepsy encephalopathy caused by KCNT1 gene mutation
Objective: To study the mutational characteristics of KCNT1 and its clinical features in children with early-onset epileptic encephalopathy. Methods: Retrospective analysis of clinical data of 175 children with early onset epilepsy from the Department of Pediatrics at Peking University First Hospita...
Ausführliche Beschreibung
Bibliographische Detailangaben
| Veröffentlicht in: | Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 56(2018), 11 vom: 02. Nov., Seite 824-828
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| 1. Verfasser: |
Chen, Y
(VerfasserIn) |
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| Weitere Verfasser: |
Bao, X H,
Zhang, Q P,
Wang, J P,
Wen, Y X,
Yu, S J,
Zhao, Y |
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| Format: | Online-Aufsatz
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| Sprache: | Chinese |
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| Veröffentlicht: |
2018
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| Zugriff auf das übergeordnete Werk: | Zhonghua er ke za zhi = Chinese journal of pediatrics
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| Schlagworte: | Journal Article
Epilepsy
Genes
Quinidine
KCNT1 protein, human
Nerve Tissue Proteins
Potassium Channels
Potassium Channels, Sodium-Activated |
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