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...

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Publié dans:	Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 60(2022), 11 vom: 02. Nov., Seite 1140-1146
Auteur principal:	Zhao, N (Auteur)
Autres auteurs:	Cheng, M M, Yang, Y, Niu, X Y, Chen, Y, Yang, X L, Zhang, Y H
Format:	Article en ligne
Langue:	Chinese
Publié:	2022
Accès à la collection:	Zhonghua er ke za zhi = Chinese journal of pediatrics
Sujets:	English Abstract Journal Article NAV1.7 Voltage-Gated Sodium Channel SCN9A protein, human