The role of renal chloride channel mutations in kidney stone disease and nephrocalcinosis.
Recent advances in molecular biology have characterised a new class of chloride channels (CLCs) that are referred to as voltage-gated CLCs. To date nine such voltage-gated CLCs (CLC-1 to CLC-7, CLC-Ka and CLC-Kb, which are encoded by the genes CLCN1 to CLCN7, CLC-Ka and CLC-Kb, respectively) have be...
Huvudupphovsman: | Thakker, R |
---|---|
Materialtyp: | Journal article |
Språk: | English |
Publicerad: |
1998
|
Liknande verk
Liknande verk
-
Hypercalciuric nephrocalcinosis in Japanese children due to mutations of the renal chloride channel (CLCN5).
av: Lloyd, SE, et al.
Publicerad: (1996) -
Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5).
av: Lloyd, SE, et al.
Publicerad: (1997) -
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.
av: Lloyd, SE, et al.
Publicerad: (1997) -
THE GENE CAUSING DENTS DISEASE, A RENAL FANCONI SYNDROME WITH NEPHROCALCINOSIS AND KIDNEY-STONES, IS ON THE SHORT ARM OF THE X-CHROMOSOME (XP11.22)
av: Thakker, R, et al.
Publicerad: (1993) -
Chloride channels in renal disease.
av: Thakker, R
Publicerad: (1999)