Exonic CLDN16 mutations associated with familial hypomagnesemia with hypercalciuria and nephrocalcinosis can induce deleterious mRNA alterations

  1. Perdomo-Ramirez, A.
  2. De Armas-Ortiz, M.
  3. Ramos-Trujillo, E.
  4. Suarez-Artiles, L.
  5. Claverie-Martin, F.
Journal:
BMC Medical Genetics

ISSN: 1471-2350

Year of publication: 2019

Volume: 20

Issue: 1

Type: Article

DOI: 10.1186/S12881-018-0713-7 GOOGLE SCHOLAR lock_openOpen access editor

Sustainable development goals

Data source: Scopus