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

Benzer Materyaller

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