ArticleClinical journal of the American Society of Nephrology : CJASN2012

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: phenotype-genotype correlation and outcome in 32 patients with CLDN16 or CLDN19 mutations.

Astrid Godron et al.PubMed ↗Full text ↗Publisher ↗

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