Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

Author:

Riedhammer Korbinian M.,Nguyen Thanh-Minh T.,Koşukcu Can,Calzada-Wack Julia,Li Yong,Batzir Nurit Assia,Saygılı Seha,Wimmers Vera,Kim Gwang-Jin,Chrysanthou Marialena,Bakey Zeineb,Sofrin-Drucker Efrat,Kraiger Markus,Sanz-Moreno Adrián,Amarie Oana V.,Rathkolb Birgit,Klein-Rodewald Tanja,Garrett Lillian,Hölter Sabine M.,Seisenberger Claudia,Haug Stefan,Schlosser Pascal,Marschall Susan,Wurst Wolfgang,Fuchs Helmut,Gailus-Durner Valerie,Wuttke Matthias,de Angelis Martin Hrabe,Ćomić Jasmina,Doğan Özlem Akgün,Özlük Yasemin,Taşdemir Mehmet,Ağbaş Ayşe,Canpolat Nur,Orenstein Naama,Çalışkan Salim,Weber Ruthild G.,Bergmann Carsten,Jeanpierre Cecile,Saunier Sophie,Lim Tze Y.,Hildebrandt Friedhelm,Alhaddad Bader,Basel-Salmon Lina,Borovitz Yael,Wu Kaman,Antony Dinu,Matschkal Julia,Schaaf Christian W.,Renders Lutz,Schmaderer Christoph,Rogg Manuel,Schell Christoph,Meitinger Thomas,Heemann Uwe,Köttgen Anna,Arnold Sebastian J.,Ozaltin Fatih,Schmidts Miriam,Hoefele Julia

Publisher

Elsevier BV

Subject

Nephrology

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