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Literaturverzeichnis
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117
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D, Brem A, Trachtman H, Griswold W, Richard GA, John E, Lifton RP
Mutations in the chloride channel gene CLCNKB, cause Bartters syndrome Typ III
Nature Gen. 17: 171-178, 1997
Sutton RA, Mavichak V, Halabe A, Wilkins GE
Bartter`s syndrome: Evidence suggested a distal tubular defect in a hypocalciuric variant of the
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in Italian patients with Gitelman syndrome
Hum. Mutat. 20: 78, 2002
Taglialatela M, Wible BA, Caporaso R, Brown AM
Specification of pore properties by the carboxyl terminus of inwardly rectifying K
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Science 264: 844-847, 1994
Tsai TD, Shuck ME, Thompson DP, Bienkowski MJ, Lee KS
Intracellular H
+
inhibits a cloned rat kidney outer medulla K
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channel expressed in Xenopus
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Am. J. Physiol. 268: C1173-C1178, 1995
Vargas R, Antignac C, Jean G, Forestier L, Niaudet P, Feldmann D, Deschênes G, Károlyi L,
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Phenotypic and genetic variability in Bartter syndrome
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Waldegger S, Jentsch TJ
Functional and structural analysis of ClC-K chloride channels involved in renal disease
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