N.T. Bech-Hansen
Department of Medical Genetics
University of Calgary
Alberta
Canada
Name/email consistency: high
- Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness. Bech-Hansen, N.T., Naylor, M.J., Maybaum, T.A., Pearce, W.G., Koop, B., Fishman, G.A., Mets, M., Musarella, M.A., Boycott, K.M. Nat. Genet. (1998)
- Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23. Bech-Hansen, N.T., Boycott, K.M., Gratton, K.J., Ross, D.A., Field, L.L., Pearce, W.G. Hum. Genet. (1998)