Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidus

Author:

van den Ouweland Ans M.W.,Dreesen Jos C.F.M.,Verdijk Marian,Knoers Nine V.A.M.,Monnens Leo A.H.,Rocchi Mariano,van Oost Bernard A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference19 articles.

1. Williams, R.H. & Henry, C. Nephrogenic diabetes insipidus: Transmitted by females and appearing during infancy in males. Ann. Intern. Med. 27, 84–95 (1947).

2. Reeves, W.B. & Andreoli, T.E. Nephrogenic diabetes insipidus. In The Metabolic Basis of Inherited Disease (eds Scriver, C.R. et al.) 1985–2011 (McGraw-Hill, New York, 1989).

3. Knoers, N. & Monnens, L.A.H., Clinical symptoms, pathogenesis, genetics and treatment. Pediatr. Nephrol. (in the press).

4. Jard, S. Vasopressin receptors. In Frontiers of Hormone Research. Vol. 13. Diabetes insipidus in man (eds Czernichow, P. & Robinson, A.G.) 89–104 (S. Karger. Basel, 1985).

5. Bichet, D.G. et al. Hemodynamic and coagulation responses to 1 -desamino[8-D-Arginine] vasopressin in patients with congenital nephrogenic diabetes insipidus. New Engl. J. Med. 318, 881–887 (1988).

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