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  • Dent s syndrome
  • Bartter s syndrome
  • CASR
  • Kidney (Inherited diseases)
  • Nephrocalcinosis
  • Hypocalciemic hypercalciuria autosomal dominant
  • Hypercalciuric nephrolithiasis with hypophosphatemia
  • Hypomagnesemia with hypercalciuria familiar
  • NPT2c
  • Paracellin1
  • ClC5
  • CLC Kb
  • OCRL1
  • CLCN5
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    12000Pathogenesis of Dent's disease and related syndromes of X-linked nephrolithiasis.



    		+-nlKidney Int 57(3):787-93 (2000)
    21998X-linked hypercalciuric nephrolithiasis: clinical syndromes and chloride channel mutations.



    		+-nlKidney Int 53(1):3-17 (1998)
    32006Recent advances in understanding the clinical and genetic heterogeneity of Dent's disease.



    		+-nlNephrol Dial Transplant 21(10):2708-17 (2006)
    42009Genetic causes of hypercalciuric nephrolithiasis.



    		+-nlPediatr Nephrol 24(12):2321-32 (2009)
    52010Dent's disease.



    		+-nlOrphanet J Rare Dis 5(-):28 (2010)



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