Case Report: A Case of Congenital Nephrogenic Diabetes Insipidus Caused by Thr273Met Mutation in Arginine Vasopressin Receptor 2

Overview of attention for article published in Frontiers in Pediatrics, July 2021

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New Research: Case Report: A Case of Congenital Nephrogenic Diabetes Insipidus Caused by Thr273Met Mutation in Arginine Vasopressin Receptor 2: Congenital nephrogenic diabetes insipidus (CNDI) is a rare hereditary tubular dysfunction caused… https://t.co/5

03 Aug 2021

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