An activating calcium sensing receptor mutation associated with normocalcemic (idiopathic) hypercalciuric nephrolithiasis.

Eitemau Tebyg

• Genetic causes of hypercalciuric nephrolithiasis.
  gan: Stechman, M, et al.
  Cyhoeddwyd: (2009)
• Genetics of hypercalciuric nephrolithiasis: renal stone disease.
  gan: Stechman, M, et al.
  Cyhoeddwyd: (2007)
• Mutations in the chloride channel gene (CLCN5) are associated with hypercalciuric rickets and nephrolithiasis.
  gan: Lloyd, SE, et al.
  Cyhoeddwyd: (1996)
• Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.
  gan: Lloyd, SE, et al.
  Cyhoeddwyd: (1997)
• Genetic analysis of the hypercalciuric rat, a model for human idiopathic hypercalciuria.
  gan: Hoopes, R, et al.
  Cyhoeddwyd: (1996)