Entries of Wutz, K. on the publication server
 | Up a level |
Number of items: 2.
2002
Wutz, K., Sauer, C., Zrenner, E., Lorenz, B., Alitalo, T., Broghammer, M., Hergersberg, M., de La Chapelle, A., Weber, Bernhard H. F. 
, Wissinger, B., Meindl, A. and Pusch, C. M.
(2002)
Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina.
European Journal of Human Genetics 10 (8), pp. 449-456.
Fulltext not available.
, Wissinger, B., Meindl, A. and Pusch, C. M.
(2002)
Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina.
European Journal of Human Genetics 10 (8), pp. 449-456.
Fulltext not available.
1998
Strom, T. M., Nyakatura, G., Apfelstedt-Sylla, E., Hellebrand, H., Lorenz, B., Weber, Bernhard H. F. , Wutz, K., Gutwillinger, N., Rüther, K., Drescher, B., Sauer, C. G., Zrenner, E., Meitinger, T., Rosenthal, A. and Meindl, A.
(1998)
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
Nature Genetics 19, pp. 260-263.
Fulltext not available.
, Wutz, K., Gutwillinger, N., Rüther, K., Drescher, B., Sauer, C. G., Zrenner, E., Meitinger, T., Rosenthal, A. and Meindl, A.
(1998)
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
Nature Genetics 19, pp. 260-263.
Fulltext not available.