Renal fibrosis is the common feature of autosomal dominant tubulointerstitial kidney diseases caused by mutations in mucin 1 or uromodulin-Reference-Cited by-同舟云学术

Renal fibrosis is the common feature of autosomal dominant tubulointerstitial kidney diseases caused by mutations in mucin 1 or uromodulin

Published:2014-09 Issue:3 Volume:86 Page:589-599
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Ekici Arif B.,Hackenbeck Thomas,Morinière Vincent,Pannes Andrea,Buettner Maike,Uebe Steffen,Janka Rolf,Wiesener Antje,Hermann Ingo,Grupp Sina,Hornberger Martin,Huber Tobias B.,Isbel Nikky,Mangos George,McGinn Stella,Soreth-Rieke Daniela,Beck Bodo B.,Uder Michael,Amann Kerstin,Antignac Corinne,Reis André,Eckardt Kai-Uwe,Wiesener Michael S.

Publisher

Elsevier BV

Subject

Nephrology

Reference34 articles.

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3. Cellular and molecular mechanisms of renal fibrosis;Liu;Nat Rev Nephrol,2011

4. Improving the recognition of hereditary interstitial kidney disease;Bleyer;J Am Soc Nephrol,2009

5. Hereditary interstitial kidney disease: known genes and opportunities for diagnosis;Srivastava;OA Nephrology,2013

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