Novel mutations of the chloride channel Kb gene in two Japanese patients clinically diagnosed as Bartter syndrome with hypocalciuria (Q28292139)

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Novel mutations of the chloride channel Kb gene in two Japanese patients clinically diagnosed as Bartter syndrome with hypocalciuria
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    Novel mutations of the chloride channel Kb gene in two Japanese patients clinically diagnosed as Bartter syndrome with hypocalciuria (English)
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    Shigeru Fukuyama
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    Misako Hiramatsu
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    Motohiro Akagi
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    Mutumi Higa
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    Takao Ohta
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    November 2004
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    89
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    11
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    5847-50
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