WCN25-3322 BARTTER’S SYNDROME TYPE II DUE TO A NOVEL MUTATION IN KCNJ1 GENE PRESENTING IN ADULTHOOD AS RECURRENT HYPOKALAEMIC PERIODIC PARALYSIS
Saved in:
| Main Authors: | , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2025-02-01
|
| Series: | Kidney International Reports |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2468024924021041 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| _version_ | 1849336173131988992 |
|---|---|
| author | Rohit Puri SHARON KANDARI |
| author_facet | Rohit Puri SHARON KANDARI |
| author_sort | Rohit Puri |
| collection | DOAJ |
| format | Article |
| id | doaj-art-1492b0261d834e59beb6c7f1eefd5b17 |
| institution | Kabale University |
| issn | 2468-0249 |
| language | English |
| publishDate | 2025-02-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Kidney International Reports |
| spelling | doaj-art-1492b0261d834e59beb6c7f1eefd5b172025-08-20T03:45:03ZengElsevierKidney International Reports2468-02492025-02-01102S6S710.1016/j.ekir.2024.11.082WCN25-3322 BARTTER’S SYNDROME TYPE II DUE TO A NOVEL MUTATION IN KCNJ1 GENE PRESENTING IN ADULTHOOD AS RECURRENT HYPOKALAEMIC PERIODIC PARALYSISRohit Puri0SHARON KANDARI1NEPHROLOGY, All india institute of medical sciences Rishikesh, Rishikesh, IndiaNEPHROLOGY, All india institute of medical sciences Rishikesh, Rishikesh, Indiahttp://www.sciencedirect.com/science/article/pii/S2468024924021041 |
| spellingShingle | Rohit Puri SHARON KANDARI WCN25-3322 BARTTER’S SYNDROME TYPE II DUE TO A NOVEL MUTATION IN KCNJ1 GENE PRESENTING IN ADULTHOOD AS RECURRENT HYPOKALAEMIC PERIODIC PARALYSIS Kidney International Reports |
| title | WCN25-3322 BARTTER’S SYNDROME TYPE II DUE TO A NOVEL MUTATION IN KCNJ1 GENE PRESENTING IN ADULTHOOD AS RECURRENT HYPOKALAEMIC PERIODIC PARALYSIS |
| title_full | WCN25-3322 BARTTER’S SYNDROME TYPE II DUE TO A NOVEL MUTATION IN KCNJ1 GENE PRESENTING IN ADULTHOOD AS RECURRENT HYPOKALAEMIC PERIODIC PARALYSIS |
| title_fullStr | WCN25-3322 BARTTER’S SYNDROME TYPE II DUE TO A NOVEL MUTATION IN KCNJ1 GENE PRESENTING IN ADULTHOOD AS RECURRENT HYPOKALAEMIC PERIODIC PARALYSIS |
| title_full_unstemmed | WCN25-3322 BARTTER’S SYNDROME TYPE II DUE TO A NOVEL MUTATION IN KCNJ1 GENE PRESENTING IN ADULTHOOD AS RECURRENT HYPOKALAEMIC PERIODIC PARALYSIS |
| title_short | WCN25-3322 BARTTER’S SYNDROME TYPE II DUE TO A NOVEL MUTATION IN KCNJ1 GENE PRESENTING IN ADULTHOOD AS RECURRENT HYPOKALAEMIC PERIODIC PARALYSIS |
| title_sort | wcn25 3322 bartter s syndrome type ii due to a novel mutation in kcnj1 gene presenting in adulthood as recurrent hypokalaemic periodic paralysis |
| url | http://www.sciencedirect.com/science/article/pii/S2468024924021041 |
| work_keys_str_mv | AT rohitpuri wcn253322bartterssyndrometypeiiduetoanovelmutationinkcnj1genepresentinginadulthoodasrecurrenthypokalaemicperiodicparalysis AT sharonkandari wcn253322bartterssyndrometypeiiduetoanovelmutationinkcnj1genepresentinginadulthoodasrecurrenthypokalaemicperiodicparalysis |