Characterization of two novel mutations in the claudin-16 and claudin-19 genes that cause familial hypomagnesemia with hypercalciuria and nephrocalcinosis

1. Perdomo-Ramirez, A.
2. Aguirre, M.
3. Davitaia, T.
4. Ariceta, G.
5. Ramos-Trujillo, E.
6. Claverie-Martin, F.