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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Detalles Bibliográficos
Autores principales: Mostofizade, Neda, Nikpour, Parvaneh, Javanmard, Shaghayegh Haghjooy, Emadi-Baygi, Modjtaba, Miranzadeh-Mahabadi, Hajar, Hovsepian, Silva, Hashemipour, Mahin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570912/
https://www.ncbi.nlm.nih.gov/pubmed/23412840

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570912/
https://www.ncbi.nlm.nih.gov/pubmed/23412840

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