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Biallelic missense variants in ZBTB11 can cause intellectual disability in humans.

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Title: Biallelic missense variants in ZBTB11 can cause intellectual disability in humans.
Authors: Fattahi Z; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Sheikh TI; Molecular Neuropsychiatry & Development (MiND) Lab, Campbell Family Mental Health Research Institute, Center for Addiction and Mental Health, Toronto, ON, Canada., Musante L; Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany., Rasheed M; Department of Biochemistry, Quaid-i-Azam University, Islamabad, Pakistan., Taskiran II; Department of Molecular Biology and Genetics, Bogazici University, Istanbul, Turkey., Harripaul R; Molecular Neuropsychiatry & Development (MiND) Lab, Campbell Family Mental Health Research Institute, Center for Addiction and Mental Health, Toronto, ON, Canada., Hu H; Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany., Kazeminasab S; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Alam MR; Department of Biochemistry, Quaid-i-Azam University, Islamabad, Pakistan., Hosseini M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Larti F; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Ghaderi Z; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Celik A; Department of Molecular Biology and Genetics, Bogazici University, Istanbul, Turkey., Ayub M; Department of Psychiatry, Queen's University, Kingston, ON, Canada., Ansar M; Department of Biochemistry, Quaid-i-Azam University, Islamabad, Pakistan., Haddadi M; Department of Biology, Faculty of Science, University of Zabol, Zabol, Iran., Wienker TF; Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany., Ropers HH; Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany., Kahrizi K; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Vincent JB; Molecular Neuropsychiatry & Development (MiND) Lab, Campbell Family Mental Health Research Institute, Center for Addiction and Mental Health, Toronto, ON, Canada., Najmabadi H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
Source: Human molecular genetics [Hum Mol Genet] 2018 Sep 15; Vol. 27 (18), pp. 3177-3188.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Biallelic missense variants in ZBTB11 can cause intellectual disability in humans.
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  Data: <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="%22Sheikh+TI%22">Sheikh TI</searchLink>; Molecular Neuropsychiatry & Development (MiND) Lab, Campbell Family Mental Health Research Institute, Center for Addiction and Mental Health, Toronto, ON, Canada.<br /><searchLink fieldCode="AU" term="%22Musante+L%22">Musante L</searchLink>; Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany.<br /><searchLink fieldCode="AU" term="%22Rasheed+M%22">Rasheed M</searchLink>; Department of Biochemistry, Quaid-i-Azam University, Islamabad, Pakistan.<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="%22Harripaul+R%22">Harripaul R</searchLink>; Molecular Neuropsychiatry & Development (MiND) Lab, Campbell Family Mental Health Research Institute, Center for Addiction and Mental Health, Toronto, ON, Canada.<br /><searchLink fieldCode="AU" term="%22Hu+H%22">Hu H</searchLink>; Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany.<br /><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="%22Alam+MR%22">Alam MR</searchLink>; Department of Biochemistry, Quaid-i-Azam University, Islamabad, Pakistan.<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="%22Larti+F%22">Larti F</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Ghaderi+Z%22">Ghaderi Z</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, 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="%22Ayub+M%22">Ayub M</searchLink>; Department of Psychiatry, Queen's University, Kingston, ON, Canada.<br /><searchLink fieldCode="AU" term="%22Ansar+M%22">Ansar M</searchLink>; Department of Biochemistry, Quaid-i-Azam University, Islamabad, Pakistan.<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="%22Wienker+TF%22">Wienker TF</searchLink>; Department of Human Molecular Genetics, Max Planck Institute for Molecular Genetics, Berlin, Germany.<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="%22Kahrizi+K%22">Kahrizi K</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.<br /><searchLink fieldCode="AU" term="%22Vincent+JB%22">Vincent JB</searchLink>; Molecular Neuropsychiatry & Development (MiND) Lab, Campbell Family Mental Health Research Institute, Center for Addiction and Mental Health, Toronto, ON, Canada.<br /><searchLink fieldCode="AU" term="%22Najmabadi+H%22">Najmabadi H</searchLink>; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
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  Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2018 Sep 15; Vol. 27 (18), pp. 3177-3188.
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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="%22IRL+Press+at+Oxford+University+Press%22">IRL Press at Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9208958 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1460-2083 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209646906%22">09646906 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mol Genet <i>Subsets: </i>MEDLINE
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