Zanoni, Paolo
Steindl, Katharina
Sengupta, Deepanwita
Joset, Pascal
Bahr, Angela
Sticht, Heinrich
Lang-Muritano, Mariarosaria
van Ravenswaaij-Arts, Conny M.A.
Shinawi, Marwan
Andrews, Marisa
Attie-Bitach, Tania
Maystadt, Isabelle
Belnap, Newell
Benoit, Valerie
Delplancq, Geoffroy
de Vries, Bert B.A.
Grotto, Sarah
Lacombe, Didier
Larson, Austin
Mourmans, Jeroen
Õunap, Katrin
Petrilli, Giulia
Pfundt, Rolph
Ramsey, Keri
Blok, Lot Snijders
Tsatsaris, Vassilis
Vitobello, Antonio
Faivre, Laurence
Wheeler, Patricia G.
Wevers, Marijke R.
Wojcik, Monica
Zweier, Markus
Gozani, Or
Rauch, Anita
Funding for this research was provided by:
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (320030_179547, 320030_179547, 320030_179547, 320030_179547)
Stanford Maternal and Child Health Research Institute (N.A.)
Eesti Teadusagentuur (PUT355)
National Human Genome Research Institute (N.A.)
National Heart, Lung, and Blood Institute (N.A. - TOPMed Program)
This article is maintained by: Elsevier
Article Title: Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-021-01158-1
Content Type: article
Copyright: © 2021, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics