The DOI matches its Crossref record; 46 of the 46 references it cites were found in a registry or an index.
Inner Ear Defects Induced by Null Mutationof the isk Gene
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Citations
Cites
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A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
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Coassembly of KVLQT1 and minK (IsK) proteins to form cardiac IKS potassium channel
Sanguinetti, M. C., Curran, M. E., Zou, A., Shen, J., Specter, P. S., Atkinson, D. L., & Keating, M. T. (1996) · Nature · doi:10.1038/384080a0 · Cited by 1,764
KvLQT1 and IsK (minK) proteins associate to form the IKS cardiac potassium current
Barhanin, J., Lesage, F., Guillemare, E., Fink, M., Lazdunski, M., & Romey, G. (1996) · Nature · doi:10.1038/384078a0 · Cited by 1,614
Self-citationJervell, A., & Lange-Nielsen, F. (1957) · American Heart Journal · doi:10.1016/0002-8703(57)90079-0 · Cited by 1,596
Genetic variants and strains of the laboratory mouse
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Characterization of a multicomponent receptor for GDNF
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Mutations in the K+ channel signature sequence
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Cited by
CLC Chloride Channels and Transporters: Structure, Function, Physiology, and Disease
Jentsch, T. J., & Pusch, M. (2018) · Physiological Reviews · doi:10.1152/physrev.00047.2017 · Cited by 448
Deafness and renal tubular acidosis in mice lacking the K-Cl co-transporter Kcc4
Boettger, T., Hübner, C. A., Maier, H., Rust, M. B., Beck, F. X., & Jentsch, T. J. (2002) · Nature · doi:10.1038/416874a · Cited by 414
Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter
Delpire, E., Lu, J., England, R., Dull, C., & Thorne, T. (1999) · Nature Genetics · doi:10.1038/9713 · Cited by 411
Roden, D. M., Balser, J. R., George Jr, A. L., & Anderson, M. E. (2002) · Annual Review of Physiology · doi:10.1146/annurev.physiol.64.083101.145105 · Cited by 305
A genetic approach to understanding auditory function
Steel, K. P., & Kros, C. J. (2001) · Nature Genetics · doi:10.1038/84758 · Cited by 290
Metadata
- Authors
- Vetter, D. E., Mann, J. R., Wangemann, P., Liu, J., McLaughlin, K. J., Lesage, F., Marcus, D. C., Lazdunski, M., Heinemann, S. F., & Barhanin, J.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 1996-12
- Volume
- 17
- Issue
- 6
- Pages
- 1251-1264
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W1990913409
- Cited by
- 403
- References
- 46
- FWCI
- 12.55
- Type
- journal article
- Language
- en
- Open access
- bronze
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How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
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- CoChat. (2026). Citation check: Inner Ear Defects Induced by Null Mutationof the isk Gene. https://app.cochat.ai/papers/10.1016/s0896-6273(00)80255-x
- The paper
- Vetter, D. E., Mann, J. R., Wangemann, P., Liu, J., McLaughlin, K. J., Lesage, F., Marcus, D. C., Lazdunski, M., Heinemann, S. F., & Barhanin, J. (1996). Inner Ear Defects Induced by Null Mutationof the isk Gene. Neuron. https://doi.org/10.1016/s0896-6273(00)80255-x
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.
