Loss-of-function truncating and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct neurodevelopmental phenotype - Zanoni, P.; Steindl, K.; Sengupta, D.; Sticht, Heinrich; Joset, P.; Baar, A.; Van Ravenswaaij-Arts, C. M. A.; Shinawi, M.; Maystadt, I.; Belnap, N.; Benoit, V.; De Vries, B. B. A.; et al. (EUROPEAN JOURNAL OF HUMAN GENETICS, 2020)
CRIS-Team WoS Importer:2021-01-22