WCN25-3322 BARTTER’S SYNDROME TYPE II DUE TO A NOVEL MUTATION IN KCNJ1 GENE PRESENTING IN ADULTHOOD AS RECURRENT HYPOKALAEMIC PERIODIC PARALYSIS

WCN25-3322 BARTTER’S SYNDROME TYPE II DUE TO A NOVEL MUTATION IN KCNJ1 GENE PRESENTING IN ADULTHOOD AS RECURRENT HYPOKALAEMIC PERIODIC PARALYSIS

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Bibliographic Details
Main Authors: Rohit Puri, SHARON KANDARI
Format: Article
Language:English
Published: Elsevier 2025-02-01
Series:Kidney International Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2468024924021041
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