A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect

MLA

Baş, Veysel Nijat, et al. “A Common Thyroid Peroxidase Gene Mutation (G319R) in Turkish Patients with Congenital Hypothyroidism Could Be Due to a Founder Effect.” Journal of Pediatric Endocrinology & Metabolism, vol. 27, no. 3–4, Mar. 2014, pp. 383–87. EBSCOhost, https://doi.org/10.1515/jpem-2013-0203.

APA

Baş, V. N., Aycan, Z., Cangul, H., Kendall, M., Ağladıoğlu, S. Y., Çetinkaya, S., & Maher, E. R. (2014). A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect. Journal of Pediatric Endocrinology & Metabolism, 27(3–4), 383–387. https://doi.org/10.1515/jpem-2013-0203

Chicago

Baş, Veysel Nijat, Zehra Aycan, Hakan Cangul, Michaela Kendall, Sebahat Yılmaz Ağladıoğlu, Semra Çetinkaya, and Eamonn R. Maher. 2014. “A Common Thyroid Peroxidase Gene Mutation (G319R) in Turkish Patients with Congenital Hypothyroidism Could Be Due to a Founder Effect.” Journal of Pediatric Endocrinology & Metabolism 27 (3–4): 383–87. doi:10.1515/jpem-2013-0203.