Loza Munarriz, R., Arias Caceres, F., & Neyra Chagua, V. (2024). Familial hypomagnesemia with hypercalciuria and nefrocalcinosis due to a mutation in the CLDN16 gen (Claudina 16). A case report.
Citación estilo ChicagoLoza Munarriz, Reyner, Fernando Arias Caceres, y Victor Neyra Chagua. Familial Hypomagnesemia With Hypercalciuria and Nefrocalcinosis Due to a Mutation in the CLDN16 Gen (Claudina 16). A Case Report. 2024.
Cita MLALoza Munarriz, Reyner, Fernando Arias Caceres, y Victor Neyra Chagua. Familial Hypomagnesemia With Hypercalciuria and Nefrocalcinosis Due to a Mutation in the CLDN16 Gen (Claudina 16). A Case Report. 2024.