Viable Ednra ^sup Y129F^ mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation von Sabrautzki, Sibylle, Sandholzer, Michael A, Lorenz-depiereux, Bettina, Brommage, Robert, Przemeck, Gerhard, Vargas Panesso, Ingrid L, Vernaleken, Alexandra, Garrett, Lillian, Baron, Katharina, Yildirim, Ali O, Rozman, Jan, Rathkolb, Birgit, Gau, Christine, Hans, Wolfgang, Hoelter, Sabine M, Marschall, Susan, Stoeger, Claudia, Becker, Lore, Fuchs, Helmut, Gailus-durner, Valerie, Klingenspor, Martin, Klopstock, Thomas, Lengger, Christoph, Stefanie, Leuchtenberger, Wolf, Eckhard, Strom, Tim M, Wurst, Wolfgang, de Angelis, Martin Hrab

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Neuron-specific inactivation of Wt1 alters locomotion in mice and changes interneuron composition in the spinal cord von Schnerwitzki, Danny, Perry, Sharn, Ivanova, Anna, Caixeta, Fabio V, Cramer, Paul, Günther, Sven, Weber, Kathrin, Tafreshiha, Atieh, Becker, Lore, Panesso, Ingrid L. Vargas, Klopstock, Thomas, Hrabe de Angelis, Martin, Schmidt, Manuela, Kullander, Klas, Englert, Christoph

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