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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Detalles Bibliográficos
Autores principales: Hashemipour, Mahin, Soheilipour, Fahimeh, Karimizare, Sakineh, Khanahmad, Hossein, Karimipour, Morteza, Aminzadeh, Sepideh, Kokabee, Leila, Amini, Massoud, Hovsepian, Silva, Hadian, Rezvaneh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Clinical Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3419406/
https://www.ncbi.nlm.nih.gov/pubmed/22919382
http://dx.doi.org/10.1155/2012/717283

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3419406/
https://www.ncbi.nlm.nih.gov/pubmed/22919382
http://dx.doi.org/10.1155/2012/717283

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