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