Haplotype analysis of CLDN19 single nucleotide polymorphisms in Spanish patients with familial hypomagnesemia with hypercalciuria and nephrocalcinosis

  1. Martin-Nuñez, E.
  2. Cordoba-Lanus, E.
  3. Gonzalez-Acosta, H.
  4. Oliet, A.
  5. Izquierdo, E.
  6. Claverie-Martin, F.
Journal:
World Journal of Pediatrics

ISSN: 1867-0687,  1708-8569

Year of publication: 2015

Volume: 11

Issue: 3

Pages: 272-275

Type: Article

DOI: 10.1007/S12519-014-0528-3 GOOGLE SCHOLAR
Data source: Scopus