Retrospective cohort study of familial hypomagnesaemia with hypercalciuria and nephrocalcinosis due to CLDN16 mutations-Reference-Cited by-同舟云学术

Retrospective cohort study of familial hypomagnesaemia with hypercalciuria and nephrocalcinosis due to CLDN16 mutations

Published:2014-12-03 Issue:4 Volume:30 Page:636-644
ISSN:0931-0509
Container-title:Nephrology Dialysis Transplantation
language:en
Short-container-title:Nephrology Dialysis Transplantation

Author:

Sikora P.,Zaniew M.,Haisch L.,Pulcer B.,Szczepa ska M.,Moczulska A.,Rogowska-Kalisz A.,Bienia B.,Tkaczyk M.,Ostalska-Nowicka D.,Zachwieja K.,Hyla-Klekot L.,Schlingmann K. P.,Konrad M.

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

Link

http://academic.oup.com/ndt/article-pdf/30/4/636/6878956/gfu374.pdf

Reference48 articles.

1. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis

2. Paracellin-1, a Renal Tight Junction Protein Required for Paracellular Mg 2+ Resorption

3. Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis maps to chromosome 3q27 and is associated with mutations in the PCLN-1 gene

4. Mutations in the Tight-Junction Gene Claudin 19 (CLDN19) Are Associated with Renal Magnesium Wasting, Renal Failure, and Severe Ocular Involvement

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