De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila

Dorien Lugtenberg, Margot R. F. Reijnders, Michaela Fenckova, Emilia K. Bijlsma, Raphael Bernier, Bregje W. M. van Bon, Eric Smeets, Anneke T. Vulto-van Silfhout, Danielle Bosch, Evan E. Eichler, Heather C. Mefford, Gemma L. Carvill, Ernie M. H. F. Bongers, Janneke H. M. Schuurs-Hoeijmakers, Claudia A. Ruivenkamp, Gijs W. E. Santen, Arn M. J. M. van den Maagdenberg, Cacha M. P. C. D. Peeters-Scholte, Sabine Kuenen, Patrik VerstrekenRolph Pfundt, Helger G. Yntema, Petra F. de Vries, Joris A. Veltman, Alexander Hoischen, Christian Gilissen, Bert B. A. de Vries, Annette Schenck, Tjitske Kleefstra, Lisenka E. L. M. Vissers

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)1145-1153
JournalEuropean Journal of Human Genetics
Volume24
Issue number8
DOIs
Publication statusPublished - Aug 2016

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