Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese.

MLA

Kanda, Keisuke, et al. “Clinical Significance of Heterozygous Carriers Associated with Compensated Hypothyroidism in R450H, a Common Inactivating Mutation of the Thyrotropin Receptor Gene in Japanese.” Endocrine, vol. 30, no. 3, Dec. 2006, pp. 383–88. EBSCOhost, https://doi.org/10.1007/s12020-006-0018-z.

APA

Kanda, K., Mizuno, H., Sugiyama, Y., Imamine, H., Togari, H., & Onigata, K. (2006). Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese. Endocrine, 30(3), 383–388. https://doi.org/10.1007/s12020-006-0018-z

Chicago

Kanda, Keisuke, Haruo Mizuno, Yukari Sugiyama, Hiroki Imamine, Hajime Togari, and Kazumichi Onigata. 2006. “Clinical Significance of Heterozygous Carriers Associated with Compensated Hypothyroidism in R450H, a Common Inactivating Mutation of the Thyrotropin Receptor Gene in Japanese.” Endocrine 30 (3): 383–88. doi:10.1007/s12020-006-0018-z.