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.
Citação norma ChicagoHanssen, 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.
ציטוט MLAHanssen, Oriane, et al. "Two Novel Mutations of the CLDN16 Gene Cause Familial Hypomagnesaemia With Hypercalciuria and Nephrocalcinosis." Clin Kidney J 2014.
אזהרה: ציטוטים אלה לעיתים לא מדויקים ב 100%.