Titre:
  • NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets
Auteur:Bouveret, Romaric; Fonoudi, Hananeh; Chen, Chiann Mun; Wouters, Merridee M.A.; Bhattacharya, Shoumo; Plachta, Nicolas; Dunwoodie, Sally S.L.; Chapman, Gavin; Blanpain, Cédric; Harvey, Richard; Waardenberg, Ashley A.J.; Schonrock, Nicole; Ramialison, Mirana; Doan, Tram; de jong, Danielle; Bondue, Antoine; Kaur, Gurpreet; Mohamed, Stephanie
Informations sur la publication:eLife, 4, JULY2015, e06942
Statut de publication:Publié, 2015-07
Sujet CREF:Sciences bio-médicales et agricoles
Neurosciences cognitives
Microbiologie et protistologie [bacteriol.,virolog.,mycolog.]
Immunologie
Note générale:SCOPUS: ar.j
Langue:Anglais
Identificateurs:urn:issn:2050-084X
info:doi/10.7554/eLife.06942
info:scp/84940567692