Author:
Addis Maria,Meloni Cristiana,Tosetto Enrica,Ceol Monica,Cristofaro Rosalba,Melis Maria Antonietta,Vercelloni Paolo,Del Prete Dorella,Marra Giuseppina,Anglani Franca
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference32 articles.
1. Wrong OM, Nordern AGW, Feest TG : Dent’s disease: a familial renal tubular syndrome with hypercalciuria, tubular proteinuria, rickets, nephrocalcinosis and eventual renal failure. Q J Med 1990; 77: 1086–1087, (Abstract).
2. Lloyd SE, Pearce SHS, Fisher SE et al: A common molecular basis for three inherited kidney stone diseases. Nature 1996; 379: 445–449.
3. Thakker RV : Pathogenesis of Dent’s disease and related syndromes of X-linked nephrolithiasis. Kidney Int 2000; 57: 787–793.
4. Gunther W, Luchow A, Cluzeaud F, Vandewalle A, Jentsch TJ : ClC-5, the chloride channel mutated in Dent’s disease, colocalizes with the proton pump in endocytotically active kidney cells. Proc Natl Acad Sci USA 1998; 95: 8075–8080.
5. Devuyst O, Christie PT, Courtoy PJ, Beauwens R, Thakker RV : Intra-renal and subcellular distribution of the human chloride channel, CLC-5 reveals a pathophysiological basis for Dent’s disease. Hum Mol Genet 1999; 8: 247–257.
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