학술논문
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
Document Type
Article
Author
Riedhammer, Korbinian M.; Nguyen, Thanh-Minh T.; Koşukcu, Can; Calzada-Wack, Julia; Li, Yong; Assia Batzir, Nurit; 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; Hrabe de Angelis, Martin; Ćomić, Jasmina; Akgün Doğan, Özlem; 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
Source
In Kidney International April 2024 105(4):844-864
Subject
Language
ISSN
0085-2538