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...
Na minha lista:
| Principais autores: | , , , , |
|---|---|
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BMC
2006-11-01
|
| Serier: | BMC Genetics |
| Online adgang: | http://www.biomedcentral.com/1471-2156/7/53 |
| Tags: |
Ingen Tags, Vær først til at tagge denne postø!
|