Low molecular weight ('tubular') proteinuria in patients with mutations of the CLCN5 renal chloride channel gene.
Egile Nagusiak: | Norden, A, Asplin, J, Deschodt-Lanckman, M, Langman, C, Lapsley, M, Nortier, J, Scheinman, S, Thakker, R, Unwin, R, Wrong, O |
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Formatua: | Journal article |
Argitaratua: |
1999
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Antzeko izenburuak
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Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.
nork: Norden, A, et al.
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Isolated hypercalciuria with mutation in CLCN5: relevance to idiopathic hypercalciuria.
nork: Scheinman, S, et al.
Argitaratua: (2000) -
Mutations in the chloride channel gene (CLCN5) are associated with hypercalciuric rickets and nephrolithiasis.
nork: Lloyd, SE, et al.
Argitaratua: (1996) -
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.
nork: Lloyd, SE, et al.
Argitaratua: (1997) -
Renal chloride channel, CLCN5, mutations in Dent's disease.
nork: Cox, J, et al.
Argitaratua: (1999)