The Vitamin D Receptor and the Syndrome of Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets*
Author:
Affiliation:
1. Department of Medicine (P.J.M., D.F.), Stanford University School of Medicine, Stanford, California 94305-5103;
2. Department of Molecular and Cellular Physiology (J.W.P.), University of Cincinnati, Cincinnati, Ohio 45267
Publisher
The Endocrine Society
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
http://academic.oup.com/edrv/article-pdf/20/2/156/10334578/edrv0156.pdf
Reference273 articles.
1. Hereditary 1,25-dihydroxyvitamin D resistant rickets: molecular basis and implications for the role of 1,25(OH)2D3 in normal physiology;Feldman;Mol Cell Endocrinol,1990
2. Genetic defects of the 1,25-dihydroxyvitamin D3 receptor.;Hughes;J Recept Res,1991
3. Hereditary 1,25-dihydroxyvitamin D resistant rickets;Malloy;In: Feldman D, Glorieux F, Pike, JW (eds) Vitamin D. Academic Press, San Diego, CA, pp,1997
4. Vitamin D;Feldman,1997
5. Vitamin-D-dependent rickets type II. Resistance of target organs to 1,25-dihydroxyvitamin D.;Brooks;N Engl J Med,1978
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