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

Những quyển sách tương tự

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