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An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
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Citations
Cited by
Structure and Regulation of Voltage-Gated Ca 2+ Channels
Catterall, W. A. (2000) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.16.1.521 · Cited by 2,344
CaV1.2 Calcium Channel Dysfunction Causes a Multisystem Disorder Including Arrhythmia and Autism
Splawski, I., Timothy, K. W., Sharpe, L. M., Decher, N., Kumar, P., Bloise, R., Napolitano, C., Schwartz, P. J., Joseph, R. M., Condouris, K., et al. (2004) · Cell · doi:10.1016/j.cell.2004.09.011 · Cited by 1,586
Bech-Hansen, N. T., Naylor, M. J., Maybaum, T. A., Pearce, W. G., Koop, B., Fishman, G. A., Mets, M., Musarella, M. A., & Boycott, K. M. (1998) · Nature Genetics · doi:10.1038/947 · Cited by 517
The diverse roles of ribbon synapses in sensory neurotransmission
Matthews, G., & Fuchs, P. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2924 · Cited by 334
RIM Binding Proteins (RBPs) Couple Rab3-Interacting Molecules (RIMs) to Voltage-Gated Ca2+ Channels
Hibino, H., Pironkova, R., Onwumere, O., Vologodskaia, M., Hudspeth, A. J., & Lesage, F. (2002) · Neuron · doi:10.1016/s0896-6273(02)00667-0 · Cited by 309
Metadata
- Authors
- 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.
- Venue
- Nature Genetics
- Published
- 1998-07
- Volume
- 19
- Issue
- 3
- Pages
- 260-263
- ISSN
- 1061-4036 (ISSN-L)
- 1546-1718
- DOI
- 10.1038/940
- OpenAlex
- W1544777143
- Cited by
- 507
- References
- 0
- FWCI
- 8.67
- Type
- journal article
- Language
- en
- Open access
- closed
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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.
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How to cite
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- This page
- CoChat. (2026). Citation check: An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness. https://app.cochat.ai/papers/10.1038/940
- The paper
- 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. https://doi.org/10.1038/940
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.
