Osteomalacia and altered magnesium metabolism in the X-linked hypophosphatemic mouse

Author:

Meyer Ralph A.,Jowsey Jenifer,Meyer Martha H.

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Orthopedics and Sports Medicine,Endocrinology, Diabetes and Metabolism

Reference32 articles.

1. Dent, C.E., Round, J.M., Stamp, T.C.B.: Treatment of sex-linked hypophosphatemic rickets (SLHR). In B. Frame, A.M. Parfitt, H. Duncan (eds.): Clincial aspects of Metabolic Bone Disease, pp. 427–432. Excerpta Medica, Amsterdam, 1973

2. Williams, T.F., Winters, R.W.: Familial (hereditary) vitamin D-resistant rickets with hypophosphatemia. In J.B. Stanbury, J.B. Wyngaarden, D.S. Fredrickson (eds.): The Metabolic Basis of Inherited Disease, pp. 1465–1485. McGraw-Hill Book Co., New York, 1972

3. Eicher, E.M., Southard, J.L., Scriver, C.R., Glorieux, F.H.: Hypophosphatemia: mouse model for human familial hypophosphatemic (vitamin D-resistant) rickets, Proc. Natl. Acad. Sci. USA73:4667–4671, 1976

4. O'Doherty, P.J.A., DeLuca, H.F., Eicher, E.M.: Lack of effect of vitamin D and its metabolites on intestinal phosphate transport in familial hypophosphatemia of mice, Endocrinology101:1325–1330, 1977

5. Meyer, R.A., Jr., Meyer, M.H.: Altered bone mineral content and composition in the X-linked hypophosphatemic (Hyp) mouse, Fed. Proc.37:436, 1978

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