Publikationen in Zusammenarbeit mit Forschern von Hospital de Cruces (3)

2023

  1. Genotypic variability in patients with clinical diagnosis of Bartter syndrome type 3

    Scientific reports, Vol. 13, Núm. 1, pp. 12587

2018

  1. URAT1 and GLUT9 mutations in Spanish patients with renal hypouricemia

    Clinica Chimica Acta, Vol. 481, pp. 83-89

2013

  1. Claudin-19 Mutations and Clinical Phenotype in Spanish Patients with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

    PLoS ONE, Vol. 8, Núm. 1