APA (7th ed.) Citation

Narumi, S., Araki, S., Hori, N., Muroya, K., Yamamoto, Y., Asakura, Y., . . . Hasegawa, T. (2012). Functional characterization of four novel PAX8 mutations causing congenital hypothyroidism: New evidence for haploinsufficiency as a disease mechanism. European journal of endocrinology, 167(5), 625-632. https://doi.org/10.1530/EJE-12-0410

Chicago Style (17th ed.) Citation

Narumi, Satoshi, Shunsuke Araki, Naoaki Hori, Koji Muroya, Yukiyo Yamamoto, Yumi Asakura, Masanori Adachi, and Tomonobu Hasegawa. "Functional Characterization of Four Novel PAX8 Mutations Causing Congenital Hypothyroidism: New Evidence for Haploinsufficiency as a Disease Mechanism." European Journal of Endocrinology 167, no. 5 (2012): 625-632. https://doi.org/10.1530/EJE-12-0410.

MLA (9th ed.) Citation

Narumi, Satoshi, et al. "Functional Characterization of Four Novel PAX8 Mutations Causing Congenital Hypothyroidism: New Evidence for Haploinsufficiency as a Disease Mechanism." European Journal of Endocrinology, vol. 167, no. 5, 2012, pp. 625-632, https://doi.org/10.1530/EJE-12-0410.