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SCN1A overexpression, associated with a genomic region marked by a risk variant for a common epilepsy, raises seizure susceptibility.

Gawel, Kinga
Tsortouktzidis, Despina
Pitsch, Julika
Alhusaini, Saud
van Loo, Karen M J
Picardo, Richard
Michalak, Zuzanna
Pagni, Susanna
Martins Custodio, Helena
Mills, James
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Abstract
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en
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1432-0533
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DOI
10.1007/s00401-022-02429-0
PMID
35551471
PMCID
PMC9217876
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