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

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, Scopus)

• 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: No