A Novel Mutation of the Arginine Vasopressin Receptor 2 Gene in a Patient with Congenital Nephrogenic Diabetes Insipidus
We have identified a novel mutation of the arginine vasopressin receptor 2 (AVPR2) gene in a case of congenital X-linked nephrogenic diabetes insipidus (NDI). The patient was a 2-mo-old Japanese boy with persistent fever and failure to thrive. He was diagnosed as having congenital NDI by clinical an...
| Main Authors: | , , , , |
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| Format: | Online |
| Language: | English |
| Published: |
The Japanese Society for Pediatric Endocrinology
2005
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4004929/ |