The role of renal chloride channel mutations in kidney stone disease and nephrocalcinosis.

Lignende værker

• Hypercalciuric nephrocalcinosis in Japanese children due to mutations of the renal chloride channel (CLCN5).
  af: Lloyd, SE, et al.
  Udgivet: (1996)
• Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).
  af: Lloyd, SE, et al.
  Udgivet: (1997)
• Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.
  af: Lloyd, SE, et al.
  Udgivet: (1997)
• THE GENE CAUSING DENTS DISEASE, A RENAL FANCONI SYNDROME WITH NEPHROCALCINOSIS AND KIDNEY-STONES, IS ON THE SHORT ARM OF THE X-CHROMOSOME (XP11.22)
  af: Thakker, R, et al.
  Udgivet: (1993)
• Chloride channels in renal disease.
  af: Thakker, R
  Udgivet: (1999)