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Reports of Biochemistry and Molecular Biology
rbmb.net
Basic Sciences
http://rbmb.net
1
admin
2322-3480
2322-3480
10.61882/rbmb
en
jalali
1398
2
1
gregorian
2019
5
1
8
1
online
1
fulltext
en
Association Study of Sequence Variants in Voltage-gated Ca2+ Channel Subunit Alpha-1C and Autism Spectrum Disorders
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. <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>
</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.