Narang, G.; Shimon, T.; Moore, J.; Hager, M.; Pinto e Vairo, F.; Stern, K.; Keddis, M.; Humphreys, M.
Novel Variant in CLDN16: A Further Step in the Diagnosis of Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis—A Case Report. Uro 2021, 1, 76-81.
https://doi.org/10.3390/uro1030011
AMA Style
Narang G, Shimon T, Moore J, Hager M, Pinto e Vairo F, Stern K, Keddis M, Humphreys M.
Novel Variant in CLDN16: A Further Step in the Diagnosis of Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis—A Case Report. Uro. 2021; 1(3):76-81.
https://doi.org/10.3390/uro1030011
Chicago/Turabian Style
Narang, Gopal, Tim Shimon, Jonathan Moore, Megan Hager, Filippo Pinto e Vairo, Karen Stern, Mira Keddis, and Mitchell Humphreys.
2021. "Novel Variant in CLDN16: A Further Step in the Diagnosis of Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis—A Case Report" Uro 1, no. 3: 76-81.
https://doi.org/10.3390/uro1030011
APA Style
Narang, G., Shimon, T., Moore, J., Hager, M., Pinto e Vairo, F., Stern, K., Keddis, M., & Humphreys, M.
(2021). Novel Variant in CLDN16: A Further Step in the Diagnosis of Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis—A Case Report. Uro, 1(3), 76-81.
https://doi.org/10.3390/uro1030011
