en زیست شناسی ملکولی Molecular Biology مقالات اصلی Original Article <div style="text-align: justify;"><strong><em>Background:</em></strong> Autism spectrum disorders (ASDs) (MIM 209850) are a group of distinct neurodevelopmental disorders characterized by impaired social interactions and communication abilities and abnormal repetitive activities. Many genetic variants have been shown to be associated with ASD. Channelopathies are among putative culprits in the pathogenesis of many neurodevelopmental disorders, including autism. The calcium channel, voltage-dependent, L type, alpha 1C subunit gene (<em>CACNA1C</em>) encodes an alpha-1 subunit of a voltage-dependent calcium channel. Genetic variants within this gene have been associated with psychiatric disorders including Autism Spectrum Disorders (ASD). Our aim was to determine whether the SNPs rs1006737, rs4765905, and rs4765913 were associated with ASD in an Iranian population. &nbsp;<br> <br> <strong><em>Methods:</em></strong> In the present case-control study we investigated the associations of rs1006737, rs4765905, and rs4765913 polymorphisms within<em> CACNA1C</em> and the risk of ASD in a population of 529 Iranian ASD patients and 480 age, gender, and ethnicity-matched healthy subjects.<br> <br> <strong><em>Results:</em></strong> None of these SNPs were associated with ASD risk in the assessed population. Although previous studies have shown an association between these polymorphisms and psychiatric disorders and an association between rs4765905 and ASD, we did not replicate those results in our study.<br> <br> <strong><em>Conclusions:</em></strong> Our data indicate that these <em>CACNA1C</em> variants are not involved in the pathogenesis of ASD in the Iranian population.<br> &nbsp;</div> Autism Spectrum Disorder, CACNA1C, Channelopathy, polymorphism. 56 62 http://rbmb.net/browse.php?a_code=A-10-187-2&slc_lang=en&sid=1 Arezou Sayad Ar.sayad@yahoo.com 100319475328460017164 100319475328460017164 No Department of Medical Genetics, Shahid Beheshti University of Medical sciences, Tehran, Iran. Soudeh Ghafouri-Fard s.ghafourifard@sbmu.ac.ir 100319475328460017165 100319475328460017165 No Department of Medical Genetics, Shahid Beheshti University of Medical sciences, Tehran, Iran. Rezvan Noroozi rezvan68noroozi@gmail.com 100319475328460017166 100319475328460017166 No Phytochemistry Research Center, Shahid Beheshti University of Medical sciences, Tehran, Iran. Mir Davood Omrani davood_omrani@yahoo.co.uk 100319475328460017167 100319475328460017167 No Department of Medical Genetics, Shahid Beheshti University of Medical sciences, Tehran, Iran & Urogenital Stem Cell Research Center, Shahid Beheshti University of Medical sciences, Tehran, Iran. Maziar Ganji maziar.ganji92@gmail.com 100319475328460017168 100319475328460017168 No Department of Medical Genetics, Shahid Beheshti University of Medical sciences, Tehran, Iran. Romina Dastmalchi romina.d@gmail.com 100319475328460017169 100319475328460017169 No Department of Medical Genetics, Shahid Beheshti University of Medical sciences, Tehran, Iran. Mark Glassy markglassy@aol.com 100319475328460017170 100319475328460017170 No Hagiwara Institute of Health Integrated Medical Sciences Association Foundation, Oceanside, CA, United States. Mohammad Taheri Mohammad_823@yahoo.com 100319475328460017171 100319475328460017171 Yes Department of Medical Genetics, Shahid Beheshti University of Medical sciences, Tehran, Iran & Urogenital Stem Cell Research Center, Shahid Beheshti University of Medical sciences, Tehran, Iran.