Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram
- Author
- C ZEITZ, M VAN GENDEREN, J NEIDHARDT, UFO LUHMANN, F HOEBEN, U FORSTER, K WYCISK, G MATYAS, CB HOYNG, F RIEMSLAG, Françoise Meire (UGent) , FPM CREMERS and W BERGER
- Organization
Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-360379
- MLA
- ZEITZ, C., et al. “Mutations in GRM6 Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram.” INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, vol. 46, no. 11, ASSOC RESEARCH VISION OPHTHALMOLOGY INC, 2005, pp. 4328–35.
- APA
- ZEITZ, C., VAN GENDEREN, M., NEIDHARDT, J., LUHMANN, U., HOEBEN, F., FORSTER, U., … BERGER, W. (2005). Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 46(11), 4328–4335.
- Chicago author-date
- ZEITZ, C, M VAN GENDEREN, J NEIDHARDT, UFO LUHMANN, F HOEBEN, U FORSTER, K WYCISK, et al. 2005. “Mutations in GRM6 Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram.” INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 46 (11): 4328–35.
- Chicago author-date (all authors)
- ZEITZ, C, M VAN GENDEREN, J NEIDHARDT, UFO LUHMANN, F HOEBEN, U FORSTER, K WYCISK, G MATYAS, CB HOYNG, F RIEMSLAG, Françoise Meire, FPM CREMERS, and W BERGER. 2005. “Mutations in GRM6 Cause Autosomal Recessive Congenital Stationary Night Blindness with a Distinctive Scotopic 15-Hz Flicker Electroretinogram.” INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE 46 (11): 4328–4335.
- Vancouver
- 1.ZEITZ C, VAN GENDEREN M, NEIDHARDT J, LUHMANN U, HOEBEN F, FORSTER U, et al. Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 2005;46(11):4328–35.
- IEEE
- [1]C. ZEITZ et al., “Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram,” INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, vol. 46, no. 11, pp. 4328–4335, 2005.
@article{360379,
author = {{ZEITZ, C and VAN GENDEREN, M and NEIDHARDT, J and LUHMANN, UFO and HOEBEN, F and FORSTER, U and WYCISK, K and MATYAS, G and HOYNG, CB and RIEMSLAG, F and Meire, Françoise and CREMERS, FPM and BERGER, W}},
issn = {{0146-0404}},
journal = {{INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE}},
language = {{eng}},
number = {{11}},
pages = {{4328--4335}},
publisher = {{ASSOC RESEARCH VISION OPHTHALMOLOGY INC}},
title = {{Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram}},
volume = {{46}},
year = {{2005}},
}