Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
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| Description | scientific journal article |
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author: Koen Van Gassen Vera M. Kalscheuer Alexander Hoischen Sarju G Mehta Stefan Haas Quinn Stein Jane Juusola Jozef Gécz Joel Charrow Frank Kooy Jolanda H Schieving Eric Haan Bregje W van Bon Han G. Brunner Usha Kini Kees E P van Roozendaal Margot R F Reijnders Céline Helsmoortel Hanka Venselaar Savanna Marie Shaw Anke Van Dijck Corinna Jensen Nataliya Di Donato A. Micheil Innes Melanie Bienek Andreas Rump Janneke H M Schuurs-Hoeijmakers Eric E Smeets Rolph Pfundt Bart L Loeys Corrado Romano Nicholas Katsanis Lisenka Vissers Tjitske Kleefstra Evan E. Eichler Lot Snijders Blok Ruth Newbury-Ecob Hilde Van Esch Christian Gilissen Diana Baralle |
| Publication date | August 6, 2015 |
| Language | English |
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