A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain

  1. Rodríguez-Soriano, J.
  2. Vallo, A.
  3. Pérez de Nanclares, G.
  4. Bilbao, J.R.
  5. Castaño, L.
Journal:
Pediatric Nephrology

ISSN: 0931-041X

Year of publication: 2005

Volume: 20

Issue: 7

Pages: 891-896

Type: Article

DOI: 10.1007/S00467-005-1867-Z GOOGLE SCHOLAR
Data source: Scopus