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Title: Molecular biology of diabetes insipidus. Author: Fujiwara TM, Morgan K, Bichet DG. Journal: Annu Rev Med; 1995; 46():331-43. PubMed ID: 7541187. Abstract: The identification, characterization, and mutational analysis of three different genes, namely the prepro-arginine-vasopressin-neurophysin II gene (prepro-AVP-NPII), the arginine-vasopressin receptor 2 gene (AVPR2), and the vasopressin-sensitive water channel gene (aquaporin-2, AQP2), provide the basis for our understanding of three different hereditary forms of diabetes insipidus: autosomal dominant neurogenic diabetes insipidus, X-linked nephrogenic diabetes insipidus, and autosomal recessive nephrogenic diabetes insipidus, respectively. These advances provide diagnostic tools for physicians caring for these patients.[Abstract] [Full Text] [Related] [New Search]