CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability-Reference-Cited by-同舟云学术

CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability

Published:2018-11-18 Issue:8 Volume:177 Page:691-699
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am J Med Genet

Author:

Kazeminasab Somayeh¹,Taskiran Ibrahim Ihsan²,Fattahi Zohreh¹,Bazazzadegan Niloofar¹,Hosseini Masoumeh¹,Rahimi Maryam¹,Oladnabi Morteza¹,Haddadi Mohammad³,Celik Arzu²,Ropers Hans-Hilger⁴,Najmabadi Hossein¹,Kahrizi Kimia¹

Affiliation:

1. Genetics Research Center; University of Social Welfare and Rehabilitation Sciences; Tehran Iran

2. Department of Molecular Biology and Genetics; Bogazici University; Istanbul Turkey

3. Department of Biology, Faculty of Science; University of Zabol; Zabol Iran

4. Department of Human Molecular Genetics; Max-Planck Institute for Molecular Genetics; Berlin Germany

Funder

Iran National Science Foundation

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics (clinical)

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.b.32648/fullpdf

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3. CNKSR2 deletions: a novel cause of X-linked intellectual disability and seizures;Aypar;American Journal of Medical Genetics Part A,2015

4. Rho GTPase signaling at the synapse: Implications for intellectual disability;Ba;Experimental Cell Research,2013

5. EphrinB1 interacts with CNK1 and promotes cell migration through c-Jun N-terminal kinase (JNK) activation;Cho;The Journal of Biological Chemistry,2014

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