Tzschach, A. Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;
Braunholz.pdf (Publisher version), 459KB
Braunholz, D., Hullings, M., Gil-Rodriguez, M. C., Fincher, C. T., Mallozzi, M. B., Loy, E., et al. (2012). Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction. European journal og human genetics: EJHG; the official journal of the European Society of Human Genetics, 20(3), 271-276. doi:10.1038/ejhg.2011.175.