ELIECER COTO GARCIA-rekin lankidetzan egindako argitalpenak (4)

2017

  1. Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome

    PLoS ONE, Vol. 12, Núm. 3

2013

  1. Dent’s disease: Identification of seven new pathogenic mutations in the CLCN5 gene

    Journal of Pediatric Genetics, Vol. 2, Núm. 3, pp. 133-140

  2. Genetics of Type III Bartter Syndrome in Spain, Proposed Diagnostic Algorithm

    PLoS ONE, Vol. 8, Núm. 9

2007

  1. Distal RTA with nerve deafness: Clinical spectrum and mutational analysis in five children

    Pediatric Nephrology, Vol. 22, Núm. 6, pp. 825-828