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Functional analysis of novel CLCNKB mutations in patients with Bartter syndrome
- Source :
- The FASEB Journal. 25
- Publication Year :
- 2011
- Publisher :
- Wiley, 2011.
-
Abstract
- Bartter’s syndrome is a hereditary renal tubulopathy characterized by salt-wasting and hypokalaemic metabolic alkalosis, which can be due to loss-of-function mutations in genes encoding ClC-Kb / Ba...
Details
- ISSN :
- 15306860 and 08926638
- Volume :
- 25
- Database :
- OpenAIRE
- Journal :
- The FASEB Journal
- Accession number :
- edsair.doi...........ea2310bf38cac011514f17282991a35b
- Full Text :
- https://doi.org/10.1096/fasebj.25.1_supplement.lb619