Hospital Severo Ochoa-ko ikertzaileekin lankidetzan egindako argitalpenak (1)

2015

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

    World Journal of Pediatrics, Vol. 11, Núm. 3, pp. 272-275