Marion Vallet

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Nicolas Picard, Pierre Meneton, Sylvie Breton, 2006 .

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

Xavier Jeunemaitre, Pierre Cochat, Marion Vallet, 2012, Clinical journal of the American Society of Nephrology : CJASN.