Cite
A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism.
MLA
Cangul, Hakan, et al. “A Truncating DUOX2 Mutation (R434X) Causes Severe Congenital Hypothyroidism.” Journal of Pediatric Endocrinology & Metabolism : JPEM, vol. 27, no. 3–4, Mar. 2014, pp. 323–27. EBSCOhost, https://doi.org/10.1515/jpem-2013-0314.
APA
Cangul, H., Aycan, Z., Kendall, M., Bas, V. N., Saglam, Y., Barrett, T. G., & Maher, E. R. (2014). A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism. Journal of Pediatric Endocrinology & Metabolism : JPEM, 27(3–4), 323–327. https://doi.org/10.1515/jpem-2013-0314
Chicago
Cangul, Hakan, Zehra Aycan, Michaela Kendall, Veysel N Bas, Yaman Saglam, Timothy G Barrett, and Eamonn R Maher. 2014. “A Truncating DUOX2 Mutation (R434X) Causes Severe Congenital Hypothyroidism.” Journal of Pediatric Endocrinology & Metabolism : JPEM 27 (3–4): 323–27. doi:10.1515/jpem-2013-0314.