Functional and pharmacological characterization of the SCN2A variant p.C258R with mixed gain and loss of function causing developmental and epileptic encephalopathy type 11.
- DOI
- 10.1016/j.ebr.2026.100897
- Published
- 2026 Dec
- Container
- Epilepsy & behavior reports
- Publisher
- Not recorded
- Open access
- yes
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BibTeX
@article{allodium:10.1016/j.ebr.2026.100897,
title = {Functional and pharmacological characterization of the SCN2A variant p.C258R with mixed gain and loss of function causing developmental and epileptic encephalopathy type 11.},
author = {Köppel A and de Vries H and Jamili M and Stanke C and Brandl U and Leipold E and Heinemann SH},
year = {2026},
journal = {Epilepsy \& behavior reports},
doi = {10.1016/j.ebr.2026.100897},
url = {https://doi.org/10.1016/j.ebr.2026.100897}
}RIS
TY - JOUR TI - Functional and pharmacological characterization of the SCN2A variant p.C258R with mixed gain and loss of function causing developmental and epileptic encephalopathy type 11. AU - Köppel A AU - de Vries H AU - Jamili M AU - Stanke C AU - Brandl U AU - Leipold E AU - Heinemann SH PY - 2026 JO - Epilepsy & behavior reports DO - 10.1016/j.ebr.2026.100897 UR - https://doi.org/10.1016/j.ebr.2026.100897 ER -
APA
A, K., H, D. V., M, J., C, S., U, B., E, L., & SH, H. (2026). Functional and pharmacological characterization of the SCN2A variant p.C258R with mixed gain and loss of function causing developmental and epileptic encephalopathy type 11.. Epilepsy & behavior reports. https://doi.org/10.1016/j.ebr.2026.100897
Source records
- pubmed · retrieved 2026-09-25T00:15:31.458Z