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.

ISSN: 1879-0038 0378-1119

Year of publication: 2019

Volume: 689

Pages: 227-234

Type: Article

DOI: 10.1016/J.GENE.2018.12.024 GOOGLE SCHOLAR

Sustainable development goals