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2. Adult presentation of Bartter syndrome type IV with erythrocytosis. Heilberg IP, Tótoli C, Calado JT. Einstein (Sao Paulo); 2015; 13(4):604-6. PubMed ID: 26537508 [Abstract] [Full Text] [Related]
3. Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome. Konrad M, Vollmer M, Lemmink HH, VAN DEN Heuvel LPWJ, Jeck N, Vargas-Poussou R, Lakings A, Ruf R, Deschênes G, Antignac C, Guay-Woodford L, Knoers NVAM, Seyberth HW, Feldmann D, Hildebrandt F. J Am Soc Nephrol; 2000 Aug; 11(8):1449-1459. PubMed ID: 10906158 [Abstract] [Full Text] [Related]
4. Generation and analyses of R8L barttin knockin mouse. Nomura N, Tajima M, Sugawara N, Morimoto T, Kondo Y, Ohno M, Uchida K, Mutig K, Bachmann S, Soleimani M, Ohta E, Ohta A, Sohara E, Okado T, Rai T, Jentsch TJ, Sasaki S, Uchida S. Am J Physiol Renal Physiol; 2011 Aug; 301(2):F297-307. PubMed ID: 21593186 [Abstract] [Full Text] [Related]
5. Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion. Estévez R, Boettger T, Stein V, Birkenhäger R, Otto E, Hildebrandt F, Jentsch TJ. Nature; 2001 Nov 29; 414(6863):558-61. PubMed ID: 11734858 [Abstract] [Full Text] [Related]
6. Atypical Bartter syndrome with sensorineural deafness with G47R mutation of the beta-subunit for ClC-Ka and ClC-Kb chloride channels, barttin. Miyamura N, Matsumoto K, Taguchi T, Tokunaga H, Nishikawa T, Nishida K, Toyonaga T, Sakakida M, Araki E. J Clin Endocrinol Metab; 2003 Feb 29; 88(2):781-6. PubMed ID: 12574213 [Abstract] [Full Text] [Related]