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. |
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| 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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