Liu, S., Han, W., Zang, Y., Zang, H., Wang, F., Jiang, P., . . . Ge, Y. (2019). Identification of Two Missense Mutations in DUOX1 (p.R1307Q) and DUOXA1 (p.R56W) That Can Cause Congenital Hypothyroidism Through Impairing H(2)O(2) Generation. Front Endocrinol (Lausanne).
Chicago-tyylinen lähdeviittausLiu, Shiguo, et al. "Identification of Two Missense Mutations in DUOX1 (p.R1307Q) and DUOXA1 (p.R56W) That Can Cause Congenital Hypothyroidism Through Impairing H(2)O(2) Generation." Front Endocrinol (Lausanne) 2019.
MLA-viiteLiu, Shiguo, et al. "Identification of Two Missense Mutations in DUOX1 (p.R1307Q) and DUOXA1 (p.R56W) That Can Cause Congenital Hypothyroidism Through Impairing H(2)O(2) Generation." Front Endocrinol (Lausanne) 2019.
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