The Vitamin D Receptor and the Syndrome of Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets*

Author:

Malloy Peter J.1,Pike J. Wesley2,Feldman David1

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

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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