Mutations of CLCN5 in Japanese children with idiopathic low molecular weight proteinuria, hypercalciuria and nephrocalcinosis.

Ítems similars

• Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).
  per: Lloyd, SE, et al.
  Publicat: (1997)
• Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuria.
  per: Scheinman, S, et al.
  Publicat: (2000)
• Hypercalciuric nephrocalcinosis in Japanese children due to mutations of the renal chloride channel (CLCN5).
  per: Lloyd, SE, et al.
  Publicat: (1996)
• Hypercalciuria and nephrocalcinosis in cystic fibrosis patients
  per: Uğur Ozçelik, et al.
  Publicat: (2004-01-01)
• Hypomagnesemia-hypercalciuria-nephrocalcinosis and ocular findings: a new claudin-19 mutation
  per: Zelal Ekinci, et al.
  Publicat: (2012-04-01)