The G395R Mutation of the Sodium/Iodide Symporter (NIS) Gene in Patients with Dyshormonogenetic Congenital Hypothyroidism

BACKGROUND: Considering the high prevalence of congenital hypothyroidism (CH) in Isfahan and its different etiologies in comparison with other countries, the high rate of parental consanguinity, and the role of NIS gene in permanent CH due to dyshormonogenesis, the aim of this study was to investiga...

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Hlavní autoři: Mostofizade, Neda, Nikpour, Parvaneh, Javanmard, Shaghayegh Haghjooy, Emadi-Baygi, Modjtaba, Miranzadeh-Mahabadi, Hajar, Hovsepian, Silva, Hashemipour, Mahin
Médium: Artigo
Jazyk:Inglês
Vydáno: Medknow Publications & Media Pvt Ltd 2013
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3570912/
https://ncbi.nlm.nih.gov/pubmed/23412840
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