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...
Spremljeno u:
| Glavni autori: | , , , , |
|---|---|
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BMC
2006-11-01
|
| Serija: | BMC Genetics |
| Online pristup: | http://www.biomedcentral.com/1471-2156/7/53 |
| Oznake: |
Bez oznaka, Budi prvi tko označuje ovaj zapis!
|