An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
10.1038/940
Crossref journal-article
Springer Science and Business Media LLC
Nature Genetics (297)
Bibliography

Strom, T. M., Nyakatura, G., Apfelstedt-Sylla, E., Hellebrand, H., Lorenz, B., Weber, B. H. F., Wutz, K., Gutwillinger, N., Rüther, K., Drescher, B., Sauer, C., Zrenner, E., Meitinger, T., Rosenthal, A., & Meindl, A. (1998). An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness. Nature Genetics, 19(3), 260–263.

Authors 15
  1. Tim M. Strom (first)
  2. Gerald Nyakatura (additional)
  3. Eckart Apfelstedt-Sylla (additional)
  4. Heide Hellebrand (additional)
  5. Birgit Lorenz (additional)
  6. Bernhard H. F. Weber (additional)
  7. Krisztina Wutz (additional)
  8. Nadja Gutwillinger (additional)
  9. Klaus Rüther (additional)
  10. Bernd Drescher (additional)
  11. Christian Sauer (additional)
  12. Eberhart Zrenner (additional)
  13. Thomas Meitinger (additional)
  14. Andre Rosenthal (additional)
  15. Alfons Meindl (additional)
References 26 Referenced 368
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  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). / Ger. J. Ophthalmol. by K Ruether (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). / Invest. Ophthalmol. Vis. Sci. by Y Miyake (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). (10.1055/s-2008-1035167) / Klin. Monatsbl. Augenheilkd by B Lorenz (1996)
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  7. Boycott, K.M. et al. Evidence for genetic heterogeneity in X-linked congenital stationary night blindness. Am. J. Hum. Genet. 62, 865– 875 (1998). (10.1086/301781) / Am. J. Hum. Genet by KM Boycott (1998)
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  26. Meindl, A. et al. A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3). Nature Genet. 13, 35–42 ( 1996). (10.1038/ng0596-35) / Nature Genet. by A Meindl (1996)
Dates
Type When
Created 23 years, 1 month ago (July 26, 2002, 4:50 a.m.)
Deposited 2 years, 3 months ago (May 18, 2023, 4:49 p.m.)
Indexed 2 hours, 52 minutes ago (Sept. 3, 2025, 6:50 a.m.)
Issued 27 years, 2 months ago (July 1, 1998)
Published 27 years, 2 months ago (July 1, 1998)
Published Print 27 years, 2 months ago (July 1, 1998)
Funders 0

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@article{Strom_1998, title={An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness}, volume={19}, ISSN={1546-1718}, url={http://dx.doi.org/10.1038/940}, DOI={10.1038/940}, number={3}, journal={Nature Genetics}, publisher={Springer Science and Business Media LLC}, author={Strom, Tim M. and Nyakatura, Gerald and Apfelstedt-Sylla, Eckart and Hellebrand, Heide and Lorenz, Birgit and Weber, Bernhard H. F. and Wutz, Krisztina and Gutwillinger, Nadja and Rüther, Klaus and Drescher, Bernd and Sauer, Christian and Zrenner, Eberhart and Meitinger, Thomas and Rosenthal, Andre and Meindl, Alfons}, year={1998}, month=jul, pages={260–263} }