DOI: 10.1055/s-00029027

Journal of Pediatric Genetics

References

Perdomo-Ramirez A, de Armas-Ortiz M, Ramos-Trujillo E, Suarez-Artiles L, Claverie-Martin F.
Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations.

BMC Med Genet 2019;
20 (01) 6

Download Bibliographical Data

Access: