Hans Eiberg
Department of Cellular and Molecular Medicine
Section IV Build. 24.4
Panum Institute
University of Copenhagen
Denmark
Name/email consistency: high
- Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression. Eiberg, H., Troelsen, J., Nielsen, M., Mikkelsen, A., Mengel-From, J., Kjaer, K.W., Hansen, L. Hum. Genet. (2008)
- Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene. Eiberg, H., Hansen, L., Kjer, B., Hansen, T., Pedersen, O., Bille, M., Rosenberg, T., Tranebjaerg, L. J. Med. Genet. (2006)
- Cholestasis Familiaris Groenlandica/Byler-like disease in Greenland--a population study. Eiberg, H., Nørgaard-Pedersen, B., Nielsen, I.M. Int. J. Circumpolar. Health (2004)