De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum.
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| Description | scientific article published on 19 October 2014 |
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author: Koen Van Gassen Joris A Veltman Marjolein H Willemsen David A Koolen Helger G Yntema Carlos A Bacino André Reis Tim M Strom Peter M van Hasselt Lisenka Vissers Hans van Bokhoven Tjitske Kleefstra Dagmar Wieczorek |
| Publication date | October 19, 2014 |
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