Salvatore, D., Dell'Edera, D., Colangelo, C., & Smaldore, G. (2016). Salt depletion syndrome as the initial presentation of cystic fibrosis in a toddler with the rare p.Ala309Gly (A309G) CFTR variant. Clinical Genetics, 90(2), 186. https://doi.org/10.1111/cge.12733
Chicago Style (17th ed.) CitationSalvatore, D., D. Dell'Edera, C. Colangelo, and G. Smaldore. "Salt Depletion Syndrome as the Initial Presentation of Cystic Fibrosis in a Toddler with the Rare P.Ala309Gly (A309G) CFTR Variant." Clinical Genetics 90, no. 2 (2016): 186. https://doi.org/10.1111/cge.12733.
MLA (9th ed.) CitationSalvatore, D., et al. "Salt Depletion Syndrome as the Initial Presentation of Cystic Fibrosis in a Toddler with the Rare P.Ala309Gly (A309G) CFTR Variant." Clinical Genetics, vol. 90, no. 2, 2016, p. 186, https://doi.org/10.1111/cge.12733.