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, 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.
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