Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

Erstveröffentlichung
2021Authors
Audain, Enrique
Wilsdon, Anna
Breckpot, Jeroen
Izarzugaza, Jose M. G.
Fitzgerald, Tomas W.
Wissenschaftlicher Artikel
Published in
PLoS Genetics ; 17 (2021), 7. - Art.-Nr. e1009679. - ISSN 1553-7404
Link to publication
https://dx.doi.org/10.1371/journal.pgen.1009679Institutions
UKU. Institut für HumangenetikSubject headings
[Free subject headings]: DE-NOVO MUTATIONS | NALCN CAUSE | DEFECTS | RISK | PREVALENCE | HYPOTONIA | GENETICS | FEATURES | NETWORK[DDC subject group]: DDC 570 / Life sciences