Associated Papers
Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Due to CLDN16 Gene Mutations: Novel Findings in Two Cases with Diverse Clinical Features.
Eltan M et al.
Calcified Tissue International, 2022
A novel claudin-16 mutation, severe bone disease, and nephrocalcinosis.
Nadarajah L et al.
Lancet (london, England), 2014
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