Missense mutation causes multiple defects in Nav1.4 channel gating and leads to an SCN4A-associated overlap phenotype.
- DOI
- 10.1085/jgp.202413706
- Published
- 2026 May 4
- Container
- The Journal of general physiology
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1085/jgp.202413706,
title = {Missense mutation causes multiple defects in Nav1.4 channel gating and leads to an SCN4A-associated overlap phenotype.},
author = {Tikhonova TB and Sharkov AA and Murtazina AF and Mashkovtseva NV and Zhorov BS and Vassilevski AA},
year = {2026},
journal = {The Journal of general physiology},
doi = {10.1085/jgp.202413706},
url = {https://doi.org/10.1085/jgp.202413706}
}RIS
TY - JOUR TI - Missense mutation causes multiple defects in Nav1.4 channel gating and leads to an SCN4A-associated overlap phenotype. AU - Tikhonova TB AU - Sharkov AA AU - Murtazina AF AU - Mashkovtseva NV AU - Zhorov BS AU - Vassilevski AA PY - 2026 JO - The Journal of general physiology DO - 10.1085/jgp.202413706 UR - https://doi.org/10.1085/jgp.202413706 ER -
APA
TB, T., AA, S., AF, M., NV, M., BS, Z., & AA, V. (2026). Missense mutation causes multiple defects in Nav1.4 channel gating and leads to an SCN4A-associated overlap phenotype.. The Journal of general physiology. https://doi.org/10.1085/jgp.202413706
Source records
- pubmed · retrieved 2026-09-26T11:22:10.968Z