Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome
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Published in American journal of human genetics (14.08.2009)
Published in American journal of human genetics (14.08.2009)
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Barttin activates ClC-K channel function by modulating gating
Fischer, Martin, Janssen, Audrey G H, Fahlke, Christoph
Published in Journal of the American Society of Nephrology (01.08.2010)
Published in Journal of the American Society of Nephrology (01.08.2010)
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