The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes
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Cites
A cluster of hydrophobic amino acid residues required for fast Na(+)-channel inactivation.
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Mutations in SCN9A, encoding a sodium channel alpha subunit, in patients with primary erythermalgia
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Self-citationContribution of Nav1.8 Sodium Channels to Action Potential Electrogenesis in DRG Neurons
Renganathan, M., Cummins, T. R., & Waxman, S. G. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.2.629 · Cited by 566
Toledo-Aral, J. J., Moss, B. L., He, Z.-J., Koszowski, A. G., Whisenand, T., Levinson, S. R., Wolf, J. J., Silos-Santiago, I., Halegoua, S., & Mandel, G. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.4.1527 · Cited by 525
Sodium channel mutations in epilepsy and other neurological disorders
Meisler, M. H. (2005) · Journal of Clinical Investigation · doi:10.1172/jci25466 · Cited by 511
Gain-of-function mutation in Nav1.7 in familial erythromelalgia induces bursting of sensory neurons
Dib-Hajj, S. D., Rush, A. M., Cummins, T. R., Hisama, F. M., Novella, S., Tyrrell, L., Marshall, L., & Waxman, S. G. (2005) · Brain · doi:10.1093/brain/awh514 · Cited by 490
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Electrophysiological Properties of Mutant Na v 1.7 Sodium Channels in a Painful Inherited Neuropathy
Cummins, T. R., Dib-Hajj, S. D., & Waxman, S. G. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.2695-04.2004 · Cited by 394
Cited by
Cellular and Molecular Mechanisms of Pain
Basbaum, A. I., Bautista, D. M., Scherrer, G., & Julius, D. (2009) · Cell · doi:10.1016/j.cell.2009.09.028 · Cited by 4,344
Colloca, L., Ludman, T., Bouhassira, D., Baron, R., Dickenson, A. H., Yarnitsky, D., Freeman, R., Truini, A., Attal, N., Finnerup, N. B., et al. (2017) · Nature Reviews Disease Primers · doi:10.1038/nrdp.2017.2 · Cited by 2,058
The Role of Voltage-Gated Sodium Channels in Pain Signaling
Bennett, D. L., Clark, A. J., Huang, J., Waxman, S. G., & Dib-Hajj, S. D. (2019) · Physiological Reviews · doi:10.1152/physrev.00052.2017 · Cited by 730
Validating therapeutic targets through human genetics
Plenge, R. M., Scolnick, E. M., & Altshuler, D. (2013) · Nature Reviews Drug Discovery · doi:10.1038/nrd4051 · Cited by 712
Sodium Channels in Normal and Pathological Pain
Dib-Hajj, S. D., Cummins, T. R., Black, J. A., & Waxman, S. G. (2010) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-153234 · Cited by 607
Metadata
- Authors
- Fertleman, C. R., Baker, M. D., Parker, K. A., Moffatt, S., Elmslie, F. V., Abrahamsen, B., Ostman, J., Klugbauer, N., Wood, J. N., Gardiner, R. M., & Rees, M.
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2006-12
- Volume
- 52
- Issue
- 5
- Pages
- 767-774
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2026551512
- Cited by
- 756
- References
- 27
- FWCI
- 13.26
- Type
- journal article
- Language
- en
- Open access
- bronze
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- CoChat. (2026). Citation check: SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes. https://app.cochat.ai/papers/10.1016/j.neuron.2006.10.006
- The paper
- Fertleman, C. R., Baker, M. D., Parker, K. A., Moffatt, S., Elmslie, F. V., Abrahamsen, B., Ostman, J., Klugbauer, N., Wood, J. N., Gardiner, R. M., & Rees, M. (2006). SCN9A Mutations in Paroxysmal Extreme Pain Disorder: Allelic Variants Underlie Distinct Channel Defects and Phenotypes. Neuron. https://doi.org/10.1016/j.neuron.2006.10.006
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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.
