학술논문
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
Document Type
Article
Author
Riedhammer, K.M.; Ćomić, J.; Alhaddad, B.; Schaaf, C.W.; Meitinger, T.; Hoefele, J.; Matschkal, J.; Renders, L.; Schmaderer, C.; Heemann, U.; Nguyen, T.-M.T.; Chrysanthou, M.; Bakey, Z.; Wu, K.; Antony, D.; Schmidts, M.; Koşukcu, C.; Ozaltin, F.; Calzada-Wack, J.; Kraiger, M.; Sanz-Moreno, A.; Amarie, O.V.; Rathkolb, B.; Klein-Rodewald, T.; Garrett, L.; Hölter, S.M.; Seisenberger, C.; Marschall, S.; Fuchs, H.; Gailus-Durner, V.; Hrabe de Angelis, M.; Li, Y.; Haug, S.; Schlosser, P.; Wuttke, M.; Köttgen, A.; Assia Batzir, N.; Sofrin-Drucker, E.; Orenstein, N.; Saygılı, S.; Ağbaş, A.; Canpolat, N.; Çalışkan, S.; Wimmers, V.; Kim, G.-J.; Arnold, S.J.; Wurst, W.; Akgün Doğan, Ö.; Özlük, Y.; Taşdemir, M.; Basel-Salmon, L.; Borovitz, Y.; Weber, R.G.; Bergmann, C.; Jeanpierre, C.; Saunier, S.; Lim, T.Y.; Hildebrandt, F.; Rogg, M.; Schell, C.
Source
In: Kidney International . (Kidney International, April 2024, 105(4):844-864)
Subject
Language
English
ISSN
15231755
00852538
00852538