Newly Identified KCNA3 Gene Variants Put the "Excite"-ment Back in Kv1.3 Channelopathy
- PMID: 38898907
- PMCID: PMC11185207
- DOI: 10.1177/15357597241234244
Newly Identified KCNA3 Gene Variants Put the "Excite"-ment Back in Kv1.3 Channelopathy
Conflict of interest statement
The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Comment on
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De novo variants in KCNA3 cause developmental and epileptic encephalopathy.Ann Neurol. 2024 Feb;95(2):365-376. doi: 10.1002/ana.26826. Epub 2023 Dec 28. Ann Neurol. 2024. PMID: 37964487
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References
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- Varanita T, Angi B, Scattolini V, Szabo I. Kv1.3 K+ channel physiology assessed by genetic and pharmacological modulation. Physiol Bethesda Md. 2023;38(1). - PubMed
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- Soldovieri MV, Ambrosino P, Mosca I, et al. De novo variants in KCNA3 cause developmental and epileptic encephalopathy. Ann Neurol. 2023;95(2):365–376. doi:10.1002/ana.26826 - PubMed
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