Inheritance of mutations in the V2 receptor gene in thirteen families with nephrogenic diabetes insipidus
- 1 July 1994
- journal article
- Published by Elsevier in Kidney International
- Vol. 46 (1), 170-176
- https://doi.org/10.1038/ki.1994.256
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Male-driven evolution of DNA sequencesNature, 1993
- Colocalization of the gene for nephrogenic diabetes insipidus (DIR) and the vasopressin type 2 receptor gene (AVPR2) in the Xq28 regionGenomics, 1992
- Cloning and characterization of a vasopressin V2 receptor and possible link to nephrogenic diabetes insipidusNature, 1992
- Molecular cloning of the receptor for human antidiuretic hormoneNature, 1992
- Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28Genomics, 1992
- Fibrinolytic Responses to 1-Desamino-8-D-Arginine-Vasopressin in Patients with Congenital Nephrogenic Diabetes insipidusNephron, 1990
- Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidusGenomics, 1989
- Nephrogenic diabetes insipidus: close linkage with markers from the distal long arm of the human X chromosomeHuman Genetics, 1988
- Hemodynamic and Coagulation Responses to 1-Desamino[8-D-Arginine] Vasopressin in Patients with Congenital Nephrogenic Diabetes InsipidusNew England Journal of Medicine, 1988
- ABSENT FACTOR VIII RESPONSE TO SYNTHETIC VASOPRESSIN ANALOGUE (DDAVP) IN NEPHROGENIC DIABETES INSIPIDUSThe Lancet, 1985