(Q48712265)
Statements
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Identification and functional analysis of novel mutations of the CLCNKB gene in Chinese patients with classic Bartter syndrome. (English)
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Y Yu
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C Xu
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X Pan
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H Ren
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W Wang
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X Meng
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F Huang
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N Chen
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6 October 2009
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77
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2
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155-162
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Identifiers
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