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1
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In memoriam: Oliver M. Wrong.

  • Scheinman, SJ, Feehally, J, Feest, TG, et al.
  • 2012-07-05
2
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Characterization of Dent's disease mutations of CLC-5 reveals a correlation between functional and cell biological consequences and protein structure.

  • Smith, AJ, Reed, AA, Loh, NY, et al.
  • 2009-02-05
3
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OCRL1 mutations in Dent 2 patients suggest a mechanism for phenotypic variability.

  • Shrimpton, AE, Hoopes, RR, Knohl, SJ, et al.
  • 2009
4
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Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).

  • Lloyd, SE, Pearce, SH, Günther, W, et al.
  • 1997-03-05
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