AMA
Sun M, Tao N, Liu X, Yang Y, Su Y, Xu F. Congenital chloride diarrhea in patient with SLC26A2 mutation – analysis of the clinical phenotype and differential diagnosis. Pediatric Endocrinology Diabetes and Metabolism. 2021;27(1):51-56. doi:10.5114/pedm.2020.97465.
APA
Sun, M., Tao, N., Liu, X., Yang, Y., Su, Y., & Xu, F. (2021). Congenital chloride diarrhea in patient with SLC26A2 mutation – analysis of the clinical phenotype and differential diagnosis. Pediatric Endocrinology Diabetes and Metabolism, 27(1), 51-56. https://doi.org/10.5114/pedm.2020.97465
Chicago
Sun, Meiyuan, Na Tao, Xiaomei Liu, Yang Yang, Yanfang Su, and Fang Xu. 2021. "Congenital chloride diarrhea in patient with SLC26A2 mutation – analysis of the clinical phenotype and differential diagnosis". Pediatric Endocrinology Diabetes and Metabolism 27 (1): 51-56. doi:10.5114/pedm.2020.97465.
Harvard
Sun, M., Tao, N., Liu, X., Yang, Y., Su, Y., and Xu, F. (2021). Congenital chloride diarrhea in patient with SLC26A2 mutation – analysis of the clinical phenotype and differential diagnosis. Pediatric Endocrinology Diabetes and Metabolism, 27(1), pp.51-56. https://doi.org/10.5114/pedm.2020.97465
MLA
Sun, Meiyuan et al. "Congenital chloride diarrhea in patient with SLC26A2 mutation – analysis of the clinical phenotype and differential diagnosis." Pediatric Endocrinology Diabetes and Metabolism, vol. 27, no. 1, 2021, pp. 51-56. doi:10.5114/pedm.2020.97465.
Vancouver
Sun M, Tao N, Liu X, Yang Y, Su Y, Xu F. Congenital chloride diarrhea in patient with SLC26A2 mutation – analysis of the clinical phenotype and differential diagnosis. Pediatric Endocrinology Diabetes and Metabolism. 2021;27(1):51-56. doi:10.5114/pedm.2020.97465.
