Deletion of the V2 vasopressin receptor gene in two Chinese patients with nephrogenic diabetes insipidus
<p>Abstract</p> <p>Background</p> <p>Congenital nephrogenic diabetes insipidus (NDI) is a rare X-linked inherited disorder characterized by the excretion of large volumes of diluted urine and caused by mutations in arginine vasopressin receptor 2 (AVPR2) gene. To investigate the mutation of AVPR2 ge...
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| Autors principals: | , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMC
2006-11-01
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| Col·lecció: | BMC Genetics |
| Accés en línia: | http://www.biomedcentral.com/1471-2156/7/53 |
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