Novel compound heterozygous mutations of CLDN16 in a patient with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

  1. García-Castaño, A.
  2. Perdomo-Ramirez, A.
  3. Vall-Palomar, M.
  4. Ramos-Trujillo, E.
  5. Madariaga, L.
  6. Ariceta, G.
  7. Claverie-Martin, F.
Molecular Genetics and Genomic Medicine

ISSN: 2324-9269

Year of publication: 2020

Volume: 8

Issue: 11

Type: Article

DOI: 10.1002/MGG3.1475 GOOGLE SCHOLAR lock_openOpen access editor

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