Thyroid Peroxidase Gene Mutation in Patients with Congenital Hypothyroidism in Isfahan, Iran

Thyroid Peroxidase Gene Mutation in Patients with Congenital Hypothyroidism in Isfahan, Iran

Background. Thyroid peroxidase gene (TPO) mutations are one of the most common causes of thyroid dyshormonogenesis in patients with congenital hypothyroidism (CH). In this study, the prevalence of TPO gene mutations in patients with thyroid dyshormonogenesis in Isfahan was investigated. Methods. In...

Full description

Saved in:
Bibliographic Details
Main Authors: Mahin Hashemipour, Fahimeh Soheilipour, Sakineh Karimizare, Hossein Khanahmad, Morteza Karimipour, Sepideh Aminzadeh, Leila Kokabee, Massoud Amini, Silva Hovsepian, Rezvaneh Hadian
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:International Journal of Endocrinology
Online Access:http://dx.doi.org/10.1155/2012/717283
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items

Similar Items