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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Detalhes bibliográficos
Main Authors: Hashemipour, Mahin, Soheilipour, Fahimeh, Karimizare, Sakineh, Khanahmad, Hossein, Karimipour, Morteza, Aminzadeh, Sepideh, Kokabee, Leila, Amini, Massoud, Hovsepian, Silva, Hadian, Rezvaneh
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2012
Assuntos:
Clinical Study
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3419406/
https://ncbi.nlm.nih.gov/pubmed/22919382
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/717283
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