Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) : report of three cases with a novel mutation in CLDN19 gene
By: al-Shibli, Ammar; Konrad, Martin; al-Atrash, Ibrahim…[et al.]. Saudi Journal of Kidney Diseases and Transplantation. Vol. 24, no. 2 (2013), pp.338-344, 7 p.
Subjects: Calcium; Case studies; Kidneys; Metabolism; Mutation