Mutation in the Tight-Junction Gene Claudin 19 (CLDN19) and Familial Hypomagnesemia, Hypercalciuria, Nephrocalcinosis (FHHNC) and Severe Ocular Disease
Author:
Publisher
S. Karger AG
Subject
Nephrology
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2. The human paracellin-1 gene (hPCLN-1): renal epithelial cell-specific expression and regulation
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4. Follow-up of five patients with FHHNC due to mutations in the Paracellin-1 gene
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