The impact of low-risk genetic variants in self-limited epilepsy with centrotemporal spikes aka Rolandic epilepsy
Research output: Contribution to journal › Comment/debate › Research
Standard
The impact of low-risk genetic variants in self-limited epilepsy with centrotemporal spikes aka Rolandic epilepsy. / Hansen, Thomas F.; Møller, Rikke S.
In: EBioMedicine, Vol. 58, 102896, 2020.Research output: Contribution to journal › Comment/debate › Research
Harvard
Hansen, TF & Møller, RS 2020, 'The impact of low-risk genetic variants in self-limited epilepsy with centrotemporal spikes aka Rolandic epilepsy', EBioMedicine, vol. 58, 102896. https://doi.org/10.1016/j.ebiom.2020.102896
APA
Hansen, T. F., & Møller, R. S. (2020). The impact of low-risk genetic variants in self-limited epilepsy with centrotemporal spikes aka Rolandic epilepsy. EBioMedicine, 58, [102896]. https://doi.org/10.1016/j.ebiom.2020.102896
Vancouver
Hansen TF, Møller RS. The impact of low-risk genetic variants in self-limited epilepsy with centrotemporal spikes aka Rolandic epilepsy. EBioMedicine. 2020;58. 102896. https://doi.org/10.1016/j.ebiom.2020.102896
Author
Bibtex
@article{4d2e969afcf74bd489368b3825dc485a,
title = "The impact of low-risk genetic variants in self-limited epilepsy with centrotemporal spikes aka Rolandic epilepsy",
keywords = "MUTATIONS",
author = "Hansen, {Thomas F.} and M{\o}ller, {Rikke S.}",
year = "2020",
doi = "10.1016/j.ebiom.2020.102896",
language = "English",
volume = "58",
journal = "EBioMedicine",
issn = "2352-3964",
publisher = "Elsevier",
}
RIS
TY - JOUR
T1 - The impact of low-risk genetic variants in self-limited epilepsy with centrotemporal spikes aka Rolandic epilepsy
AU - Hansen, Thomas F.
AU - Møller, Rikke S.
PY - 2020
Y1 - 2020
KW - MUTATIONS
U2 - 10.1016/j.ebiom.2020.102896
DO - 10.1016/j.ebiom.2020.102896
M3 - Comment/debate
C2 - 32702638
VL - 58
JO - EBioMedicine
JF - EBioMedicine
SN - 2352-3964
M1 - 102896
ER -
ID: 250123467