Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
Titel:
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
Auteur:
Snijders Blok, Lot Madsen, Erik Juusola, Jane Gilissen, Christian Baralle, Diana Reijnders, Margot R.F. Venselaar, Hanka Helsmoortel, Céline Cho, Megan T. Hoischen, Alexander Vissers, Lisenka E.L.M. Koemans, Tom S. Wissink-Lindhout, Willemijn Eichler, Evan E. Romano, Corrado Van Esch, Hilde Stumpel, Connie Vreeburg, Maaike Smeets, Eric Oberndorff, Karin van Bon, Bregje W.M. Shaw, Marie Gecz, Jozef Haan, Eric Bienek, Melanie Jensen, Corinna Loeys, Bart L. Van Dijck, Anke Innes, A. Micheil Racher, Hilary Vermeer, Sascha Di Donato, Nataliya Rump, Andreas Tatton-Brown, Katrina Parker, Michael J. Henderson, Alex Lynch, Sally A. Fryer, Alan Ross, Alison Vasudevan, Pradeep Kini, Usha Newbury-Ecob, Ruth Chandler, Kate Male, Alison Dijkstra, Sybe Schieving, Jolanda Giltay, Jacques van Gassen, Koen L.I. Schuurs-Hoeijmakers, Janneke Tan, Perciliz L. Pediaditakis, Igor Haas, Stefan A. Retterer, Kyle Reed, Patrick Monaghan, Kristin G. Haverfield, Eden Natowicz, Marvin Myers, Angela Kruer, Michael C. Stein, Quinn Strauss, Kevin A. Brigatti, Karlla W. Keating, Katherine Burton, Barbara K. Kim, Katherine H. Charrow, Joel Norman, Jennifer Foster-Barber, Audrey Kline, Antonie D. Kimball, Amy Zackai, Elaine Harr, Margaret Fox, Joyce McLaughlin, Julie Lindstrom, Kristin Haude, Katrina M. van Roozendaal, Kees Brunner, Han Chung, Wendy K. Kooy, R. Frank Pfundt, Rolph Kalscheuer, Vera Mehta, Sarju G. Katsanis, Nicholas Kleefstra, Tjitske