APA aipamena

Hanssen, O., Castermans, E., Bovy, C., Weekers, L., Erpicum, P., Dubois, B., . . . Jouret, F. (2014). Two novel mutations of the CLDN16 gene cause familial hypomagnesaemia with hypercalciuria and nephrocalcinosis. Clin Kidney J.

Chicago Style aipamena

Hanssen, Oriane, Emilie Castermans, Christophe Bovy, Laurent Weekers, Pauline Erpicum, Bernard Dubois, Vincent Bours, Jean-Marie Krzesinski, and François Jouret. "Two Novel Mutations of the CLDN16 Gene Cause Familial Hypomagnesaemia With Hypercalciuria and Nephrocalcinosis." Clin Kidney J 2014.

MLA aipamena

Hanssen, Oriane, et al. "Two Novel Mutations of the CLDN16 Gene Cause Familial Hypomagnesaemia With Hypercalciuria and Nephrocalcinosis." Clin Kidney J 2014.