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CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability.

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Title: CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability.
Authors: Kazeminasab S; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Taskiran II; Department of Molecular Biology and Genetics, Bogazici University, Istanbul, Turkey., Fattahi Z; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Bazazzadegan N; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Hosseini M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Rahimi M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Oladnabi M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Haddadi M; Department of Biology, Faculty of Science, University of Zabol, Zabol, Iran., Celik A; Department of Molecular Biology and Genetics, Bogazici University, Istanbul, Turkey., Ropers HH; Department of Human Molecular Genetics, Max-Planck Institute for Molecular Genetics, Berlin, Germany., Najmabadi H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Kahrizi K; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Source: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics [Am J Med Genet B Neuropsychiatr Genet] 2018 Dec; Vol. 177 (8), pp. 691-699. Date of Electronic Publication: 2018 Nov 18.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235742 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-485X (Electronic) Linking ISSN: 15524841 NLM ISO Abbreviation: Am J Med Genet B Neuropsychiatr Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability.
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  Data: <searchLink fieldCode="AU" term="%22Kazeminasab+S%22">Kazeminasab S</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Taskiran+II%22">Taskiran II</searchLink>; Department of Molecular Biology and Genetics, Bogazici University, Istanbul, Turkey.<br /><searchLink fieldCode="AU" term="%22Fattahi+Z%22">Fattahi Z</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Bazazzadegan+N%22">Bazazzadegan N</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Hosseini+M%22">Hosseini M</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Rahimi+M%22">Rahimi M</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Oladnabi+M%22">Oladnabi M</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Haddadi+M%22">Haddadi M</searchLink>; Department of Biology, Faculty of Science, University of Zabol, Zabol, Iran.<br /><searchLink fieldCode="AU" term="%22Celik+A%22">Celik A</searchLink>; Department of Molecular Biology and Genetics, Bogazici University, Istanbul, Turkey.<br /><searchLink fieldCode="AU" term="%22Ropers+HH%22">Ropers HH</searchLink>; Department of Human Molecular Genetics, Max-Planck Institute for Molecular Genetics, Berlin, Germany.<br /><searchLink fieldCode="AU" term="%22Najmabadi+H%22">Najmabadi H</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Kahrizi+K%22">Kahrizi K</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
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  Data: <searchLink fieldCode="JN" term="%22101235742%22">American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics</searchLink> [Am J Med Genet B Neuropsychiatr Genet] 2018 Dec; Vol. 177 (8), pp. 691-699. <i>Date of Electronic Publication: </i>2018 Nov 18.
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  Data: Journal Article; Research Support, Non-U.S. Gov't
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Blackwell%22">Wiley-Blackwell </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101235742 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1552-485X (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215524841%22">15524841 </searchLink><i>NLM ISO Abbreviation: </i>Am J Med Genet B Neuropsychiatr Genet <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=30450701
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        Value: 10.1002/ajmg.b.32648
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              Text: 2018 Dec
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