Clinical features of KCNB1 gene variation related developmental and epileptic encephalopathy
Objective: To summarize the clinical features of epilepsy and (or) developmental delay associated with KCNB1 gene variants in children. Methods: A case series study was conducted on 24 children with KCNB1 gene variants associated with epilepsy and (or) developmental delay who were treated at the Chi...
Ausführliche Beschreibung
Bibliographische Detailangaben
| Veröffentlicht in: | Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 62(2024), 11 vom: 02. Nov., Seite 1064-1070
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| 1. Verfasser: |
Zeng, Q
(VerfasserIn) |
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| Weitere Verfasser: |
Yang, Y,
Cheng, M M,
Wang, T,
Tan, Q Z,
Liu, C H,
Yang, X L,
Liao, J X,
Zhang, Y H |
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| Format: | Online-Aufsatz
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| Sprache: | Chinese |
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| Veröffentlicht: |
2024
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| Zugriff auf das übergeordnete Werk: | Zhonghua er ke za zhi = Chinese journal of pediatrics
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| Schlagworte: | English Abstract
Journal Article
KCNB1 protein, human
Shab Potassium Channels |
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