Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations
- Perdomo-Ramirez, A.
- De Armas-Ortiz, M.
- Ramos-Trujillo, E.
- Suarez-Artiles, L.
- Claverie-Martin, F.
Aldizkaria:
BMC Medical Genetics
ISSN: 1471-2350
Argitalpen urtea: 2019
Alea: 20
Zenbakia: 1
Mota: Artikulua
