A, M., D, B., O, G., L, M., X, I., M, C., . . . P, C. (2011). Loss-of-function point mutations associated with renal tubular dysgenesis provide insights about renin function and cellular trafficking. Human molecular genetics, 20(2), 301. https://doi.org/10.1093/hmg/ddq465
Chicago Style (17th ed.) CitationA, Michaud, Bur D, Gribouval O, Muller L, Iturrioz X, Clemessy M, Gasc JM, Gubler MC, and Corvol P. "Loss-of-function Point Mutations Associated with Renal Tubular Dysgenesis Provide Insights About Renin Function and Cellular Trafficking." Human Molecular Genetics 20, no. 2 (2011): 301. https://doi.org/10.1093/hmg/ddq465.
MLA (9th ed.) CitationA, Michaud, et al. "Loss-of-function Point Mutations Associated with Renal Tubular Dysgenesis Provide Insights About Renin Function and Cellular Trafficking." Human Molecular Genetics, vol. 20, no. 2, 2011, p. 301, https://doi.org/10.1093/hmg/ddq465.