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...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Hashemipour, Mahin, Soheilipour, Fahimeh, Karimizare, Sakineh, Khanahmad, Hossein, Karimipour, Morteza, Aminzadeh, Sepideh, Kokabee, Leila, Amini, Massoud, Hovsepian, Silva, Hadian, Rezvaneh
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Hindawi Publishing Corporation 2012
Aiheet:
Clinical Study
Linkit: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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