Genotype-phenotype implications from three representative clinical FOXG1 variants associated with FOXG1 syndrome

被引：2
|
作者：
Bai, Yan [1 ]
Yi, Aiwen [1 ]
Xin, Jing [1 ]
Xu, Jiaxin [1 ]
Huang, Mingwei [2 ]
机构：
[1] Chancheng Cent Hosp, Foshan, Peoples R China
[2] Aegicare Shenzhen Technol Co Ltd, Shenzhen, Peoples R China
来源：
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY | 2021年 / 89卷
关键词：
FOXG1; syndrome; Genotype-phenotype relationship; General developmental delay; Seizures; Clinical heterogeneity;
D O I：
10.1016/j.seizure.2021.04.023
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
[No abstract available]
引用
收藏
页码：45 / 47
页数：3
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