Viable EdnraY129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation.
Document type:
Zeitschriftenaufsatz
Author(s):
Sabrautzki, S. ; Sandholzer, M.A. ; Lorenz-Depiereux, B. ; Brommage, R. ; Przemeck, G.K.H. ; Vargas Panesso, I.L. ; Vernaleken, A. ; Garrett, L. ; Baron, K. ; Yildirim, A.Ö. ; Rozman, J. ; Rathkolb, B. ; Gau, C. ; Hans, W. ; Hölter, S. ; Marschall, S. ; Stöger, C. ; Becker, L. ; Fuchs, H. ; Gailus-Durner, V. ; Klingenspor, M. ; Klopstock, T. ; Lengger, C. ; Stefanie, L. ; Wolf, E. ; Strom, T.M. ; Wurst, W. ; Hrabé de Angelis, M.
Research Programmes: Genes and Environment in Common Diseases ; German Center for Diabetes Research ; Research Units: Research Unit Comparative Medicine (AVM)
TUM Institution:
Institute of Experimental Genetics (IEG) ; Institute of Human Genetics (IHG) ; Institute of Developmental Genetics (IDG) ; Institute of Lung Biology (ILBD)