Entries of Rüther, K. on the publication server
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Number of items: 2.
2017
Schulz, H. L., Grassmann, F. 
, Kellner, U., Spital, G., Rüther, K., Jägle, H., Hufendiek, K., Rating, P. and Weber, Bernhard H. F.
(2017)
Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs.
Investigative Ophthalmology & Visual Science (IOVS) 58, pp. 394-403.
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.