Berger, Wolfgang Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;
Rehm, H. L., Zhang, D.-S., Brown, M. C., Burgess, B., Halpin, C., Berger, W., et al. (2002). Vascular Defects and Sensorineural Deafness in a Mouse Model of Norrie Disease. Journal of Neuroscience, 22(11), 4286-4292.