Identification of LBX2 as a novel causal gene of atrial septal defect
Wang, Jing1; Luo, Jing2; Chenc, Qiuhong3; Wang, Xi4; He, Jiangyan5; Zhang, Wei4; Yin, Zhan5; Zheng, Fang2; Pan, Hong4; Li, Tengyan4; Lou, Qiyong5; Wang, Binbin4
2018-08-15
Source PublicationINTERNATIONAL JOURNAL OF CARDIOLOGY
ISSN0167-5273
Volume265Pages:188-194
AbstractBackground: Atrial septal defect (ASD) is one of the most common cardiac malformations worldwide. Several genes have been identified so far, which can merely explain small proportion of all the cases, therefore, it is anticipated that there are additional genes causing ASD. The aims of this study were to identify the causal gene of ostium secundum atrial septal defect (ASDII) in a Chinese family.
SubtypeArticle
KeywordAtrial Septal Defect Lbx2 Neural Crest Cells Whole Exome Sequencing
DOI10.1016/j.ijcard.2018.04.038
WOS HeadingsScience & Technology ; Life Sciences & Biomedicine
Indexed BySCI
Funding OrganizationNational Natural Science Foundation of China(81400243 ; National Natural Science Foundation of China(81400243 ; Hi-Tech Research and Development Program of China (863 Programs)(2012AA022402) ; Hi-Tech Research and Development Program of China (863 Programs)(2012AA022402) ; 81300131) ; 81300131) ; National Natural Science Foundation of China(81400243 ; National Natural Science Foundation of China(81400243 ; Hi-Tech Research and Development Program of China (863 Programs)(2012AA022402) ; Hi-Tech Research and Development Program of China (863 Programs)(2012AA022402) ; 81300131) ; 81300131)
Language英语
WOS Research AreaCardiovascular System & Cardiology
WOS SubjectCardiac & Cardiovascular Systems
WOS KeywordCONGENITAL HEART-DISEASE ; CARDIAC NEURAL CREST ; UROGENITAL SYSTEM ; RISK-FACTORS ; MUTATIONS ; CELLS ; ZEBRAFISH ; MIGRATION ; PAX3 ; ASSOCIATION
WOS IDWOS:000434679400040
Funding OrganizationNational Natural Science Foundation of China(81400243 ; National Natural Science Foundation of China(81400243 ; Hi-Tech Research and Development Program of China (863 Programs)(2012AA022402) ; Hi-Tech Research and Development Program of China (863 Programs)(2012AA022402) ; 81300131) ; 81300131) ; National Natural Science Foundation of China(81400243 ; National Natural Science Foundation of China(81400243 ; Hi-Tech Research and Development Program of China (863 Programs)(2012AA022402) ; Hi-Tech Research and Development Program of China (863 Programs)(2012AA022402) ; 81300131) ; 81300131)
Citation statistics
Document Type期刊论文
Identifierhttp://ir.ihb.ac.cn/handle/342005/50867
Collection藻类生物学及应用研究中心_水生生物分子与细胞生物学研究中心
Affiliation1.Capital Med Univ, Sch Basic Med Sci, Dept Med Genet & Dev Biol, Beijing 100069, Peoples R China
2.Wuhan Univ, Zhongnan Hosp, Ctr Gene Diag, Wuhan 430071, Hubei, Peoples R China
3.Qinghai High Altitude Med Res Inst, Cardiovasc Ctr, Xining 810012, Peoples R China
4.Natl Res Inst Family Planning, Ctr Genet, Beijing 100081, Peoples R China
5.Chinese Acad Sci, Inst Hydrobiol, Key Lab Aquat Biodivers & Conservat, Wuhan 430072, Hubei, Peoples R China
Recommended Citation
GB/T 7714
Wang, Jing,Luo, Jing,Chenc, Qiuhong,et al. Identification of LBX2 as a novel causal gene of atrial septal defect[J]. INTERNATIONAL JOURNAL OF CARDIOLOGY,2018,265:188-194.
APA Wang, Jing.,Luo, Jing.,Chenc, Qiuhong.,Wang, Xi.,He, Jiangyan.,...&Wang, Binbin.(2018).Identification of LBX2 as a novel causal gene of atrial septal defect.INTERNATIONAL JOURNAL OF CARDIOLOGY,265,188-194.
MLA Wang, Jing,et al."Identification of LBX2 as a novel causal gene of atrial septal defect".INTERNATIONAL JOURNAL OF CARDIOLOGY 265(2018):188-194.
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