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...

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Xehetasun bibliografikoak
Egile Nagusiak: Mahin Hashemipour, Fahimeh Soheilipour, Sakineh Karimizare, Hossein Khanahmad, Morteza Karimipour, Sepideh Aminzadeh, Leila Kokabee, Massoud Amini, Silva Hovsepian, Rezvaneh Hadian
Formatua: Artikulua
Hizkuntza:English
Argitaratua: Hindawi Limited 2012-01-01
Saila:International Journal of Endocrinology
Sarrera elektronikoa:http://dx.doi.org/10.1155/2012/717283

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