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

Παρόμοια τεκμήρια

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