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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Detalles Bibliográficos
Autores principales: Dong, Yan, Sheng, Haihui, Chen, Xueru, Yin, Jun, Su, Qing
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1657029/
https://www.ncbi.nlm.nih.gov/pubmed/17101063
http://dx.doi.org/10.1186/1471-2156-7-53

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1657029/
https://www.ncbi.nlm.nih.gov/pubmed/17101063
http://dx.doi.org/10.1186/1471-2156-7-53

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