Biophysical and structural mechanisms of epilepsy-associated mutations in the S4-S5 Linker of KCNQ2 channels
Mutations in KCNQ2 are linked to various neurological disorders, including neonatal-onset epilepsy. The severity of these conditions often correlates with the mutation’s location and the biochemical properties of the altered amino acid side chains. Two mutations affecting aspartate at position 212 (...
Furkejuvvon:
| Váldodahkkit: | , , , , |
|---|---|
| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Taylor & Francis Group
2025-12-01
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| Ráidu: | Channels |
| Fáttát: | |
| Liŋkkat: | https://www.tandfonline.com/doi/10.1080/19336950.2025.2464735 |
| Fáddágilkorat: |
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