Saisawat, P., Kohl, S., Hilger, A. C., Hwang, D.-Y., Gee, H. Y., Dworschak, G. C., Tasic, V., Pennimpede, T., Natarajan, S.,
Sperry, E., Matassa, D. S., Stajic, N., Bogdanovic, R., de Blaauw, I., Marcelis, C. L. M., Wijers, C. H. W., Bartels, E.,
Schmiedeke, E., Schmidt, D., Märzheuser, S., Grasshoff-Derr, S., Holland-Cunz, S., Ludwig, M., Nöthen, M. M., Draaken, M.,
Brosens, E., Heij, H., Tibboel, D., Hermann, B. G., Solomon, B. D., de Klein, A., van Rooij, I. A. L. M., Esposito, F., Reutter,
H. M., & Hildebrandt, F. (2014). Whole-exome resequencing reveals recessive mutations
in TRAP1 in individuals with CAKUT and VACTERL association. Kidney International, 85(6), 1310-1317. doi:10.1038/ki.2013.417.
