R434X Mutation in Dual Oxidase 2 Gene among Patients with Permanent and Transient Congenital Hypothyroidism

Background: The prevalence of congenital hypothyroidism (CH) is high in Isfahan (Iran). Considering the high rate of parental consanguinity and the role of dual oxidase 2 (DUOX2) gene in transient and permanent CH due to thyroid dyshormonogenesis, the aim of this research was to investigate the R434...

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Bibliographic Details

Published in:	مجله دانشکده پزشکی اصفهان
Main Authors:	Omid Khoshnoud, Mohammad Hassan Tajaddini, Mahin Hashemipour, Mansour Salehi, Awat Feizi, Shaghayegh Haghjooy Javanmard, Roya Kelishadi, Silva Hovsepian, Masoud Amini
Format:	Article
Language:	Persian
Published:	Isfahan University of Medical Sciences 2012-12-01
Online Access:	http://jims.mui.ac.ir/index.php/jims/article/view/2278