Mechanisms of Disease: the kidney-specific chloride channels ClCKA and ClCKB, the Barttin subunit, and their clinical relevance
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,General Medicine
Link
http://www.nature.com/articles/ncpneph0689.pdf
Reference52 articles.
1. Simon DB et al. (1997) Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III. Nature Genet 17: 171–178
2. Matsumara M et al. (1999) Overt nephrogenic diabetes insipidus in mice lacking the CLC-K1 chloride channel. Nature Genet 21: 95–98
3. Birkenhäger R et al. (2001) Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure. Nat Genet 29: 310–314
4. Schlingmann KP et al. (2004) Salt wasting and deafness resulting from mutations in two chloride channels. N Engl J Med 350: 1314–1319
5. Uchida S et al. (1993) Molecular cloning of a chloride channel that is regulated by dehydration and expressed predominantly in kidney medulla. J Biol Chem 268: 3821–3824
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