Open AccessClinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes
Author(s) -
Tülay Güran,
Teoman Akçay,
Abdullah Bereket,
Zeynep Atay,
Serap Turan,
L. Haisch,
Moira Konrad,
Karl P. Schlingmann
Publication year - 2011
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/gfr300
Subject(s) - nephrocalcinosis , hypercalciuria , medicine , hypocalcaemia , endocrinology , hypomagnesemia , parathyroid hormone , population , magnesium deficiency (plants) , gastroenterology , tetany , pediatrics , kidney , calcium , magnesium , chemistry , organic chemistry , environmental health
Recent identification and characterization of novel renal Mg(2+) transporters and ion channels have greatly increased our understanding of the normal physiology of renal magnesium handling.
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