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Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability.

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Title: Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability.
Authors: van der Werf IM; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium., Van Dijck A; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium., Reyniers E; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium., Helsmoortel C; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium., Kumar AA; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium., Kalscheuer VM; Research Group Development and Disease, Max Planck Institute for Molecular Genetics, Berlin, Germany., de Brouwer AP; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands., Kleefstra T; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands., van Bokhoven H; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands., Mortier G; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium., Janssens S; Center for Medical Genetics Ghent, Ghent University, Ghent University Hospital, Ghent, Belgium., Vandeweyer G; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium., Kooy RF; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium. Electronic address: Frank.Kooy@uantwerpen.be.
Source: Gene [Gene] 2017 Mar 20; Vol. 605, pp. 92-98. Date of Electronic Publication: 2016 Dec 16.
Publication Type: Journal Article
Journal Info: Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-0038 (Electronic) Linking ISSN: 03781119 NLM ISO Abbreviation: Gene Subsets: MEDLINE
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  Data: Mutations in two large pedigrees highlight the role of ZNF711 in X-linked intellectual disability.
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  Data: <searchLink fieldCode="AU" term="%22van+der+Werf+IM%22">van der Werf IM</searchLink>; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium.<br /><searchLink fieldCode="AU" term="%22Van+Dijck+A%22">Van Dijck A</searchLink>; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium.<br /><searchLink fieldCode="AU" term="%22Reyniers+E%22">Reyniers E</searchLink>; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium.<br /><searchLink fieldCode="AU" term="%22Helsmoortel+C%22">Helsmoortel C</searchLink>; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium.<br /><searchLink fieldCode="AU" term="%22Kumar+AA%22">Kumar AA</searchLink>; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium.<br /><searchLink fieldCode="AU" term="%22Kalscheuer+VM%22">Kalscheuer VM</searchLink>; Research Group Development and Disease, Max Planck Institute for Molecular Genetics, Berlin, Germany.<br /><searchLink fieldCode="AU" term="%22de+Brouwer+AP%22">de Brouwer AP</searchLink>; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Kleefstra+T%22">Kleefstra T</searchLink>; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22van+Bokhoven+H%22">van Bokhoven H</searchLink>; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Mortier+G%22">Mortier G</searchLink>; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium.<br /><searchLink fieldCode="AU" term="%22Janssens+S%22">Janssens S</searchLink>; Center for Medical Genetics Ghent, Ghent University, Ghent University Hospital, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Vandeweyer+G%22">Vandeweyer G</searchLink>; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium.<br /><searchLink fieldCode="AU" term="%22Kooy+RF%22">Kooy RF</searchLink>; Department of Medical Genetics, University of Antwerp and University Hospital Antwerp, Antwerp, Belgium. Electronic address: Frank.Kooy@uantwerpen.be.
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  Data: <searchLink fieldCode="JN" term="%227706761%22">Gene</searchLink> [Gene] 2017 Mar 20; Vol. 605, pp. 92-98. <i>Date of Electronic Publication: </i>2016 Dec 16.
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