CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia
CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia
About this item
Full title
Author / Creator
For the China Epilepsy Gene 1.0 Project , China Epilepsy Gene 1.0 Project , Liu, Xiao‐Rong , Ye, Ting‐Ting , Zhang, Wen‐Jun , Guo, Xuan , Wang, Jie , Huang, Shao‐Ping , Xie, Long‐Shan , Song, Xing‐Wang , Deng, Wei‐Wen , Li, Bing‐Mei , He, Na , Wu, Qian‐Yi , Zhuang, Min‐Zhi , Xu, Meng , Shi, Yi‐Wu , Su, Tao , Yi, Yong‐Hong and Liao, Wei‐Ping
Publisher
England: John Wiley & Sons, Inc
Journal title
Language
English
Formats
Publication information
Publisher
England: John Wiley & Sons, Inc
Subjects
More information
Scope and Contents
Contents
Aims
CHD4 gene, encoding chromodomain helicase DNA‐binding protein 4, is a vital gene for fetal development. In this study, we aimed to explore the association between CHD4 variants and idiopathic epilepsy.
Methods
Trios‐based whole‐exome sequencing was performed in a cohort of 482 patients with childhood idiopathic epilepsy. The Clinical...
Alternative Titles
Full title
CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia
Authors, Artists and Contributors
Author / Creator
China Epilepsy Gene 1.0 Project
Liu, Xiao‐Rong
Ye, Ting‐Ting
Zhang, Wen‐Jun
Guo, Xuan
Wang, Jie
Huang, Shao‐Ping
Xie, Long‐Shan
Song, Xing‐Wang
Deng, Wei‐Wen
Li, Bing‐Mei
He, Na
Wu, Qian‐Yi
Zhuang, Min‐Zhi
Xu, Meng
Shi, Yi‐Wu
Su, Tao
Yi, Yong‐Hong
Liao, Wei‐Ping
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8446219
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8446219
Other Identifiers
ISSN
1755-5930
E-ISSN
1755-5949
DOI
10.1111/cns.13692
