Mutations in the chloride channel gene (CLCN5) are associated with hypercalciuric rickets and nephrolithiasis.

相似书籍

• Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.
  由: Lloyd, SE, et al.
  出版: (1997)
• Hypercalciuric nephrocalcinosis in Japanese children due to mutations of the renal chloride channel (CLCN5).
  由: Lloyd, SE, et al.
  出版: (1996)
• HEREDITARY NEPHROLITHIASIS IS ASSOCIATED WITH MUTATIONS IN AN X-LINKED CHLORIDE CHANNEL GENE
  由: Lloyd, S, et al.
  出版: (1995)
• Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).
  由: Lloyd, SE, et al.
  出版: (1997)
• Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis).
  由: Fisher, S, et al.
  出版: (1995)