A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects.

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Cangul H., Bas V. N., Saglam Y., Kendall M., Barrett T., Maher E., ...More

Journal of pediatric endocrinology & metabolism : JPEM, vol.27, pp.1101-5, 2014 (SCI-Expanded)

• Publication Type: Article / Article
• Volume: 27
• Publication Date: 2014
• Doi Number: 10.1515/jpem-2014-0025
• Journal Name: Journal of pediatric endocrinology & metabolism : JPEM
• Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
• Page Numbers: pp.1101-5
• Kütahya Health Sciences University Affiliated: Yes