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 invest...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
BMC
2006-11-01
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| Series: | BMC Genetics |
| Online Access: | http://www.biomedcentral.com/1471-2156/7/53 |