Association between Common Single- nucleotide Polymorphism of Reelin Gene, rs736707 (C/T) with Autism Spectrum Disorder in Iranian-Azeri Patients

Association between Common Single- nucleotide Polymorphism of Reelin Gene, rs736707 (C/T) with Autism Spectrum Disorder in Iranian-Azeri Patients

Introduction Reelin gene (RELN) codes a large extracellular matrix glycoprotein with serine protease activity and is implicated in the modulation of neuronal signaling, synaptic transmission and plasticity. The reelin plays a fundamental and pivotal role in the development of laminar structures and...

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Bibliographic Details
Main Authors: Leila Mehdizadeh Fanid, Hassan Shahrokhi, Mina Adampourezare, Mohamad Ali Hosseinpour Feizi, Mortaza Bonyadi, A Eslami
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2015-11-01
Series:International Journal of Pediatrics
Subjects:
Autism
Molecular marker, Polymorphism, Reelin gene
Online Access:http://ijp.mums.ac.ir/pdf_5668_36645997f394194bd88af5a72cad1c9b.html

Internet

http://ijp.mums.ac.ir/pdf_5668_36645997f394194bd88af5a72cad1c9b.html

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