A <i>de novo</i> KCNQ2 Gene Mutation Associated With Non-familial Early Onset Seizures: Case Report and Revision of Literature Data.

导出 LinkOut

翻译打印收藏纠错

作者： Gianluigi,Laccetta ^[1] ; Simona,Fiori ^[2] ; Matteo,Giampietri ^[1] ; Annarita,Ferrari ^[2] ; Valentina,Cetica ^[3] ; Manuela,Bernardini ^[1] ; Francesca,Chesi ^[1] ; Sara,Mazzotti ^[2] ; Elena,Parrini ^[3] ; Massimiliano,Ciantelli ^[1] ; Andrea,Guzzetta ^[2] ; Paolo,Ghirri ^[4]

作者单位： Division of Neonatology and Neonatal Intensive Care Unit, Department of Maternal and Child Health, Santa Chiara Hospital, University of Pisa, Pisa, Italy. ^[1] Department of Developmental Neuroscience, IRCCS Stella Maris, Pisa, Italy. ^[2] Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Neuroscience Department, Meyer Children's University Hospital, University of Florence, Florence, Italy. ^[3] Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy. ^[4]

关键词 KCNQ2 benign familial neonatal convulsions mutation phenobarbital seizures

DOI 10.3389/fped.2019.00348

PMID 31552204

发布时间 2020-09-30

翻译满意度评价：

准确一般字义偏差语意偏离译文作用小提交

浏览0

Frontiers in pediatrics

2019年7卷

348页

相似文献

中文期刊
外文期刊
学位论文
会议论文

检索历史清除

A <i>de novo</i> KCNQ2 Gene Mutation Associated With Non-familial Early Onset Seizures: Case Report and Revision of Literature Data.

Frontiers in pediatrics

相似文献

Frontiers in pediatrics

相关期刊

参考文献：
指定格式：	NoteExpress EndNote RefWorks NoteFirst

检索历史 清除

A <i>de novo</i> KCNQ2 Gene Mutation Associated With Non-familial Early Onset Seizures: Case Report and Revision of Literature Data.

Frontiers in pediatrics

相似文献

Frontiers in pediatrics

相关期刊

检索历史清除