Low molecular weight ('tubular') proteinuria in patients with mutations of the CLCN5 renal chloride channel gene.

Samankaltaisia teoksia

• Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.
  Tekijä: Norden, A, et al.
  Julkaistu: (2000)
• Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuria.
  Tekijä: Scheinman, S, et al.
  Julkaistu: (2000)
• Mutations in the chloride channel gene (CLCN5) are associated with hypercalciuric rickets and nephrolithiasis.
  Tekijä: Lloyd, SE, et al.
  Julkaistu: (1996)
• Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.
  Tekijä: Lloyd, SE, et al.
  Julkaistu: (1997)
• Renal chloride channel, CLCN5, mutations in Dent's disease.
  Tekijä: Cox, J, et al.
  Julkaistu: (1999)