Loss-of-function truncating and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct neurodevelopmental phenotype

P. Zanoni, K. Steindl, D. Sengupta, H. Sticht, P. Joset, A. Baar, C. M. A. van Ravenswaaij-Arts, M. Shinawi, I. Maystadt, N. Belnap, V. Benoit, B. B. A. de Vries, D. Lacombe, A. Larson, R. Pfundt, K. Ramsey, L. Snijders Blok, P. G. Wheeler, M. R. Wevers, O. GozaniA. Rauch

Research output: Contribution to journalMeeting AbstractAcademic

Original languageEnglish
Pages (from-to)355-356
Number of pages2
JournalEuropean Journal of Human Genetics
Issue numberSUPPL 1
Publication statusPublished - Dec-2020

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