An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

Author:

Strom Tim M.,Nyakatura Gerald,Apfelstedt-Sylla Eckart,Hellebrand Heide,Lorenz Birgit,Weber Bernhard H. F.,Wutz Krisztina,Gutwillinger Nadja,Rüther Klaus,Drescher Bernd,Sauer Christian,Zrenner Eberhart,Meitinger Thomas,Rosenthal Andre,Meindl Alfons

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference26 articles.

1. Schubert, G. & Bornschein, H. Beitrag zur Analyse des menschlichen Electroretinogramms. Ophthalmologica 123, 396–413 (1952).

2. Ruether, K., Apfelstedt-Sylla, E. & Zrenner, E. Clinical findings in patients with congenital stationary night blindness of the Schubert-Bornschein type. Ger. J. Ophthalmol. 2 , 429–435 (1993).

3. Miyake, Y., Horiuchi, M., Ota, I. & Shiroyama, N. Characteristic ERG flicker anomaly in incomplete congenital stationary night blindness. Invest. Ophthalmol. Vis. Sci. 28, 1816– 1823 (1987).

4. Lorenz, B., Andrassi, M. & Miliczek, K.D. Die inkomplette kongenitale stationäre Nachtblindheit (CSNB). Eine wichtige Differentialdiagnose des kongenitalen Nystagmus. Klin. Monatsbl. Augenheilkd. 208, 48– 55 (1996).

5. Bergen, A.A.B., ten Brink, J.B., Riemslag, F., Schuurman, E.J.M. & Tijmes N. Localization of a novel X-linked congenital stationary night blindness locus: Close linkage to the RP3 type retinitis pigmentosa gene region. Hum. Mol. Genet. 4, 931–935 (1995).

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