The DOI matches its Crossref record; 14 of the 14 references it cites were found in a registry or an index.
Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel
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Citations
Cites
Structure and Function of Cyclic Nucleotide-Gated Channels
Zagotta, W. N., & Siegelbaum, S. A. (1996) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.19.030196.001315 · Cited by 497
Coburn, C. M., & Bargmann, C. I. (1996) · Neuron · doi:10.1016/s0896-6273(00)80201-9 · Cited by 438
Dryja, T. P., Berson, E. L., Rao, V. R., & Oprian, D. D. (1993) · Nature Genetics · doi:10.1038/ng0793-280 · Cited by 341
Dryja, T. P., Finn, J. T., Peng, Y. W., McGee, T. L., Berson, E. L., & Yau, K. W. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.22.10177 · Cited by 277
Payne, A. (1998) · Human Molecular Genetics · doi:10.1093/hmg/7.2.273 · Cited by 234
Rod and cone photoreceptor cells express distinct genes for cGMP-gated channels
Bönigk, W., Altenhofen, W., Müller, F., Dose, A., Illing, M., Molday, R. S., & Kaupp, U. B. (1993) · Neuron · doi:10.1016/0896-6273(93)90202-3 · Cited by 228
Baumann, A., Frings, S., Godde, M., Seifert, R., & Kaupp, U. B. (1994) · The EMBO Journal · doi:10.1002/j.1460-2075.1994.tb06833.x · Cited by 180
Fain, G., & Lisman, J. E. (1993) · Experimental Eye Research · doi:10.1006/exer.1993.1132 · Cited by 150
Semple‐Rowland, S. L., Lee, N., Hooser, J. P. V., Palczewski, K., & Baehr, W. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.3.1271 · Cited by 133
Pittler, S. J., Lee, A. K., Altherr, M. R., Howard, T. A., Seldin, M. F., Hurwitz, R. L., Wasmuth, J. J., & Baehr, W. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)42689-0 · Cited by 112
Cited by
McBee, J. K., Palczewski, K., Baehr, W., & Pepperberg, D. R. (2001) · Progress in Retinal and Eye Research · doi:10.1016/s1350-9462(01)00002-7 · Cited by 366
Abu-Safieh, L., Alrashed, M., Anazi, S., Alkuraya, H., Khan, A. O., Al-Owain, M., Al-Zahrani, J., Al-Abdi, L., Hashem, M., Al-Tarimi, S., et al. (2013) · Genome Research · doi:10.1101/gr.144105.112 · Cited by 276
Simunovic, M. P. (2010) · Eye · doi:10.1038/eye.2009.251 · Cited by 276
A comprehensive review of retinal gene therapy
Boye, S. E., Boye, S. L., Lewin, A. S., & Hauswirth, W. W. (2013) · Molecular Therapy · doi:10.1038/mt.2012.280 · Cited by 262
Molecular Genetics of Human Retinal Disease
Rattner, A., Sun, H., & Nathans, J. (1999) · Annual Review of Genetics · doi:10.1146/annurev.genet.33.1.89 · Cited by 228
Metadata
- Authors
- Kohl, S., Marx, T., Giddings, I., Jägle, H., Jacobson, S. G., Apfelstedt-Sylla, E., Zrenner, E., Sharpe, L. T., & Wissinger, B.
- Venue
- Nature Genetics
- Published
- 1998-07
- Volume
- 19
- Issue
- 3
- Pages
- 257-259
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- DOI
- 10.1038/935
- OpenAlex
- W1799877731
- Cited by
- 340
- References
- 14
- FWCI
- 3.83
- Type
- journal article
- Language
- en
- Open access
- closed
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel. https://app.cochat.ai/papers/10.1038/935
- The paper
- Kohl, S., Marx, T., Giddings, I., Jägle, H., Jacobson, S. G., Apfelstedt-Sylla, E., Zrenner, E., Sharpe, L. T., & Wissinger, B. (1998). Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel. Nature Genetics. https://doi.org/10.1038/935
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
