MUTATION ANALYSIS OF THE NRXN1 GENE
IN AUTISM SPECTRUM DISORDERS
Onay H1, Kacamak D, Kavasoglu AN, Akgun B, Yalcinli M, Kose S, Ozbaran B
*Corresponding Author: Huseyin Onay, M.D., Ph.D., Department of Medical Genetics, Ege University School of
Medicine, Bornova, Izmir, Turkey. Tel: +90-232-3903961. Fax: +90-232-3903971. E-mail: onayhuseyin@ gmail.com;
huseyin.onay@ege.edu.tr
page: 17
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ACKNOWLEDGMENTS
All authors contributed equally to this study: H.O.
designed the study; B.O., S.K. and D.K. made patients’
autism diagnosis; H.O., A.K., M.Y. and B.A. performed
the NRXN1 gene. All authors discussed the results on the
manuscript at all stages.
Declaration of Interest. This study was supported by
Ege University Scientific Research Projects Committee.
The authors report no conflicts of interest. The authors alone
are responsible for the content and writing of this article.
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