A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism.

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Cangul H., Aycan Z., Kendall M., Bas V. N. , Saglam Y., Barrett T., ...More

Journal of pediatric endocrinology & metabolism : JPEM, vol.27, pp.323-7, 2014 (SCI-Expanded)

• Publication Type: Article / Article
• Volume: 27
• Publication Date: 2014
• Doi Number: 10.1515/jpem-2013-0314
• Journal Name: Journal of pediatric endocrinology & metabolism : JPEM
• Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
• Page Numbers: pp.323-7
• Kütahya Health Sciences University Affiliated: Yes