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

Παρόμοια τεκμήρια

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