Hanno Bolz
Institute of Human Genetics
University Hospital of Cologne
Cologne
Germany
Name/email consistency: high
- Protocadherin-21 (PCDH21), a candidate gene for human retinal dystrophies. Bolz, H., Ebermann, I., Gal, A. Mol. Vis. (2005)
- Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11). Bolz, H., Bolz, S.S., Schade, G., Kothe, C., Mohrmann, G., Hess, M., Gal, A. Hum. Mutat. (2004)