APA (7th ed.) Citation

M, V., C, B., F, C., A, M., & G, A. (2021). Heterogeneity is a common ground in familial hypomagnesemia with hypercalciuria and nephrocalcinosis caused by CLDN19 gene mutations. Journal of nephrology, 34(6), 2053. https://doi.org/10.1007/s40620-021-01054-6

Chicago Style (17th ed.) Citation

M, Vall-Palomar, Burballa C, Claverie-Martín F, Meseguer A, and Ariceta G. "Heterogeneity Is a Common Ground in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Caused by CLDN19 Gene Mutations." Journal of Nephrology 34, no. 6 (2021): 2053. https://doi.org/10.1007/s40620-021-01054-6.

MLA (9th ed.) Citation

M, Vall-Palomar, et al. "Heterogeneity Is a Common Ground in Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Caused by CLDN19 Gene Mutations." Journal of Nephrology, vol. 34, no. 6, 2021, p. 2053, https://doi.org/10.1007/s40620-021-01054-6.