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. |
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| 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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| ISSN: | 1460-2083 |
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| DOI: | 10.1093/hmg/ddy220 |
