Article thumbnail
Location of Repository

Variants in CUL4B are Associated with Cerebral Malformations

By Anneke T. Vulto-van Silfhout, Tadashi Nakagawa, Nadia Bahi-Buisson, Stefan A. Haas, Hao Hu, Melanie Bienek, Lisenka E. L. M. Vissers, Christian Gilissen, Andreas Tzschach, Andreas Busche, Joerg Muesebeck, Patrick Rump, Inge B. Mathijssen, Kristiina Avela, Mirja Somer, Fatma Doagu, Anju K. Philips, Anita Rauch, Alessandra Baumer, Krysta Voesenek, Karine Poirier, Jacqueline Vigneron, Daniel Amram, Sylvie Odent, Magdalena Nawara, Ewa Obersztyn, Jacek Lenart, Agnieszka Charzewska, Nicolas Lebrun, Ute Fischer, Willy M. Nillesen, Helger G. Yntema, Irma Jarvela, Hans-Hilger Ropers, Bert B. A. de Vries, Han G. Brunner, Hans van Bokhoven, F. Lucy Raymond, Michel A. A. P. Willemsen, Jamel Chelly, Yue Xiong, A. James Barkovich, Vera M. Kalscheuer, Tjitske Kleefstra and Arjan P. M. de Brouwer
Topics: CUL4B, WDR62, cortical dysplasia, hydrocephalus, intellectual disability, mutation, LINKED MENTAL-RETARDATION, UBIQUITIN E3 LIGASE, SHORT STATURE, INTELLECTUAL DISABILITY, PROTEIN, MUTATIONS, GENE, DELETION, FAMILY
Year: 2015
DOI identifier: 10.1002/humu.22718
OAI identifier: oai:pure.rug.nl:publications/5148910d-8a7a-4f37-abc3-d8137af33667
Download PDF:
Sorry, we are unable to provide the full text but you may find it at the following location(s):
  • https://doi.org/10.1002/humu.2... (external link)
  • https://www.rug.nl/research/po... (external link)
  • http://hdl.handle.net/11370/51... (external link)
  • Suggested articles


    To submit an update or takedown request for this paper, please submit an Update/Correction/Removal Request.