Nephrolithiasis, kidney failure and bone disorders in Dent disease patients with and without CLCN5 mutations.

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第一作者： Franca,Anglani

第一单位： Division of Nephrology, Department of Medicine DIMED, Laboratory of Histomorphology and Molecular Biology of the Kidney, University of Padua, Via Giustiniani n° 2, 35128 Padua, Italy.

作者： Franca,Anglani ^[1] ; Angela,D'Angelo ^[1] ; Luisa Maria,Bertizzolo ^[1] ; Enrica,Tosetto ^[1] ; Monica,Ceol ^[1] ; Daniela,Cremasco ^[1] ; Luciana,Bonfante ^[1] ; Maria Antonietta,Addis ^[2] ; Dorella,Del Prete ^[1] ; Dent Disease Italian Network

作者单位： Division of Nephrology, Department of Medicine DIMED, Laboratory of Histomorphology and Molecular Biology of the Kidney, University of Padua, Via Giustiniani n° 2, 35128 Padua, Italy. ^[1] Department of Public Health, Clinical and Molecular Medicine, University of Cagliari, Cagliari, Italy. ^[2]

关键词 CLCN5 gene Calcium phosphate metabolism Chronic kidney disease Dent disease Nephrolithiasis OCRL gene

DOI 10.1186/s40064-015-1294-y

PMID 26389017

发布时间 2020-10-01

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Nephrolithiasis, kidney failure and bone disorders in Dent disease patients with and without CLCN5 mutations.

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Nephrolithiasis, kidney failure and bone disorders in Dent disease patients with and without CLCN5 mutations.

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