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Deletion of the V2 vasopressin receptor gene in two Chinese patients with nephrogenic diabetes insipidus
BACKGROUND: 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 gene in a Chinese family wi...
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| 主要な著者: | , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2006
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1657029/ https://ncbi.nlm.nih.gov/pubmed/17101063 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-7-53 |
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