Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).

Samankaltaisia teoksia

• Hypercalciuric nephrocalcinosis in Japanese children due to mutations of the renal chloride channel (CLCN5).
  Tekijä: Lloyd, SE, et al.
  Julkaistu: (1996)
• Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis.
  Tekijä: Akuta, N, et al.
  Julkaistu: (1997)
• Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.
  Tekijä: Lloyd, SE, et al.
  Julkaistu: (1997)
• Mutations in the chloride channel gene (CLCN5) are associated with hypercalciuric rickets and nephrolithiasis.
  Tekijä: Lloyd, SE, et al.
  Julkaistu: (1996)
• Functional characterization of renal chloride channel, CLCN5, mutations associated with Dent'sJapan disease.
  Tekijä: Igarashi, T, et al.
  Julkaistu: (1998)