Systems genetics analysis identifies calcium-signaling defects as novel cause of congenital heart disease

被引：0
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作者：
Jose M. G. Izarzugaza
Sabrina G. Ellesøe
Canan Doganli
Natasja Spring Ehlers
Marlene D. Dalgaard
Enrique Audain
Gregor Dombrowsky
Karina Banasik
Alejandro Sifrim
Anna Wilsdon
Bernard Thienpont
Jeroen Breckpot
Marc Gewillig
J. David Brook
Marc-Phillip Hitz
Lars A. Larsen
Søren Brunak
机构：
[1] Technical University of Denmark,Department of Health Technology
[2] University of Copenhagen,Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences
[3] University of Copenhagen,Department of Cellular and Molecular Medicine
[4] Technical University of Denmark,DTU Multi Assay Core (DMAC)
[5] Universitätsklinikum Schleswig–Holstein Kiel,Department of Congenital Heart Disease and Pediatric Cardiology
[6] Wellcome Trust Sanger Institute,Centre for Human Genetics
[7] Katholieke Universiteit Leuven,School of Life Sciences
[8] University of Nottingham,Genetics and Genome Biology
[9] Hospital for Sick Children,Pediatric Cardiology Unit
[10] University Hospitals Leuven,undefined
[11] Institute of Human Genetics,undefined
[12] Christian-Albrechts-University Kiel & University Hospital Schleswig-Holstein,undefined
[13] Campus Kiel,undefined
来源：
Genome Medicine | / 12卷
关键词：
Congenital heart disease; Genetics; Whole exome sequencing; Developmental biology; Systems biology; Calcium signaling;
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