DUOX2 variants are a frequent cause of congenital primary hypothyroidism in Thai patients

OBJECTIVE: To identify the genetic etiologies of congenital primary hypothyroidism (CH) in Thai patients. DESIGN AND METHODS: CH patients were enrolled. Clinical characteristics including age, signs and symptoms of CH, pedigree, family history, screened thyroid-stimulating hormone results, thyroid f...

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Detalles Bibliográficos
Autores principales: Sorapipatcharoen, Kinnaree, Tim-Aroon, Thipwimol, Mahachoklertwattana, Pat, Chantratita, Wasun, Iemwimangsa, Nareenart, Sensorn, Insee, Panthan, Bhakbhoom, Jiaranai, Poramate, Noojarern, Saisuda, Khlairit, Patcharin, Pongratanakul, Sarunyu, Suprasongsin, Chittiwat, Korwutthikulrangsri, Manassawee, Sriphrapradang, Chutintorn, Poomthavorn, Preamrudee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7774760/
https://www.ncbi.nlm.nih.gov/pubmed/33310921
http://dx.doi.org/10.1530/EC-20-0411

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7774760/
https://www.ncbi.nlm.nih.gov/pubmed/33310921
http://dx.doi.org/10.1530/EC-20-0411

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