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pro vyhledávání: '"Antje Wiesener"'
Autor:
Michael Uder, Kai-Uwe Eckardt, Kerstin Amann, George Mangos, Daniela Soreth-Rieke, Corinne Antignac, Bodo B. Beck, Ingo Hermann, Tobias B. Huber, Maike Buettner, Arif B. Ekici, Michael S. Wiesener, Stella McGinn, Steffen Uebe, Martin Hornberger, Thomas Hackenbeck, Antje Wiesener, Andrea Pannes, Sina Grupp, André Reis, N. M. Isbel, Vincent Morinière, Rolf Janka
Publikováno v:
Kidney international. 86(3)
For decades, ill-defined autosomal dominant renal diseases have been reported, which originate from tubular cells and lead to tubular atrophy and interstitial fibrosis. These diseases are clinically indistinguishable, but caused by mutations in at le