The Mutation of Dual Oxidase 2 (DUOX2) Gene among Patients with Permanent and Transient Congenital Hypothyroidism

The Mutation of Dual Oxidase 2 (DUOX2) Gene among Patients with Permanent and Transient Congenital Hypothyroidism

Background: Considering the high prevalence of congenital hypothyroidism (CH) in Isfahan and its different etiologies comparing with other countries, the high rate of parental consanguinity and the role of DUOX2 gene in transient CH and permanent CH due to dyshormonogenesis, the aim of this research...

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Bibliographic Details
Main Authors: Nooshin Rostampour, Mohamadhasan Tajaddini, Mahin Hashemipour, Mansour Salehi, Avat Feizi, Shaghayegh Haghjooy Javanmard, Roya Kelishadi, Hosein Saneian, Silva Hovsepian, Massoud Amini
Format: Article
Language:fas
Published: Isfahan University of Medical Sciences 2011-07-01
Series:مجله دانشکده پزشکی اصفهان
Subjects:
Congenital Hypothyroidism
Dual Oxidase 2 (DUOX2) gene
Online Access:http://jims.mui.ac.ir/index.php/jims/article/view/1083

Internet

http://jims.mui.ac.ir/index.php/jims/article/view/1083

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