Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
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author: Lot Snijders Blok, Diana Baralle, Hanka Venselaar, Céline Helsmoortel, Lisenka Vissers, Corrado Romano, Jozef Gécz, Bart L Loeys, Anke Van Dijck, Nataliya Di Donato, Koen Van Gassen, Stefan Haas, Quinn Stein, Frank Kooy, Vera M. Kalscheuer, Eric E Smeets, Han G. Brunner, Evan E. Eichler, Usha Kini, Ruth Newbury-Ecob, Eric Haan, Savanna Marie Shaw, Melanie Bienek, Corinna Jensen, Bregje W van Bon, Hilde Van Esch, Kees E P van Roozendaal, Nicholas Katsanis, Tjitske Kleefstra, Andreas Rump, Rolph Pfundt, A. Micheil Innes, Jolanda H Schieving, Jane Juusola, Margot R F Reijnders, Janneke H M Schuurs-Hoeijmakers, Christian Gilissen, Alexander Hoischen, Sarju G Mehta, Joel Charrow
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