Genetics and clinical phenotypes of epilepsy associated with chromosome 2q24.3 microdeletion
Objective: To summarize the genetics and clinical phenotypes of epilepsy children with 2q24.3 microdeletion. Methods: All the patients with 2q24.3 microdeletion were retrospectively collected at the Pediatric Department of Peking University First Hospital from March 2017 to July 2022. The features o...
Ausführliche Beschreibung
Bibliographische Detailangaben
| Veröffentlicht in: | Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 60(2022), 11 vom: 02. Nov., Seite 1140-1146
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| 1. Verfasser: |
Zhao, N
(VerfasserIn) |
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| Weitere Verfasser: |
Cheng, M M,
Yang, Y,
Niu, X Y,
Chen, Y,
Yang, X L,
Zhang, Y H |
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| Format: | Online-Aufsatz
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| Sprache: | Chinese |
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| Veröffentlicht: |
2022
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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
NAV1.7 Voltage-Gated Sodium Channel
SCN9A protein, human |
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