Clinical and Functional Characterization of a Novel Mutation in AVPR2 Causing Nephrogenic Diabetes Insipidus in a Four-Generation Chinese Family

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

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New Research: Clinical and Functional Characterization of a Novel Mutation in AVPR2 Causing Nephrogenic Diabetes Insipidus in a Four-Generation Chinese Family: Background: Congenital nephrogenic diabetes insipidus (CNDI) is a rare inherited… https://t.co/e

15 Jan 2022

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Clinical and Functional Characterization of a Novel Mutation in AVPR2 Causing Nephrogenic Diabetes Insipidus in a Four-Generation Chinese Family https://t.co/vFwxDif8bV

28 Dec 2021

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RT @ASPNeph: Clinical and Functional Characterization of a Novel Mutation in AVPR2 Causing Nephrogenic Diabetes Insipidus in a Four-Generat…

12 Dec 2021

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Clinical and Functional Characterization of a Novel Mutation in AVPR2 Causing Nephrogenic Diabetes Insipidus in a Four-Generation Chinese Family https://t.co/2PSMiChYvl @FrontPediatrics

11 Dec 2021

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