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Publications by Wutz, K

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Jump to: 2002 | 1998
Number of items: 2.


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.


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.

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