학술논문
De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila
Document Type
Article
Author
Lugtenberg, D.; Reijnders, M.R.F.; Fenckova, M.; Van Bon, B.W.M.; Vulto-van Silfhout, A.T.; Bosch, D.; Bongers, E.M.H.F.; Schuurs-Hoeijmakers, J.H.M.; Pfundt, R.; Yntema, H.G.; De Vries, P.F.; Veltman, J.A.; Hoischen, A.; Gilissen, C.; De Vries, B.B.A.; Schenck, A.; Kleefstra, T.; Vissers, L.E.L.M.; Bijlsma, E.K.; Ruivenkamp, C.A.; Santen, G.W.E.; Van Den Maagdenberg, A.M.J.M.; Bernier, R.; Smeets, E.; Eichler, E.E.; Mefford, H.C.; Carvill, G.L.; Peeters-Scholte, C.M.P.C.D.; Kuenen, S.; Verstreken, P.
Source
In: European Journal of Human Genetics . (European Journal of Human Genetics, 1 August 2016, 24(8):1145-1153)
Subject
Language
English
ISSN
14765438
10184813
10184813