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Paper Details

Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures.
Nat Commun
111
2015
EIMFS, KCC2, KCC2 dysfunction, SLC12A5, SLC12A5 mutations, chloride, epilepsy, epilepsy of infancy, epilepsy of infancy with migrating focal seizures, epilepsy syndrome, epileptic encephalopathy, human, infantile-onset, patients, potassium, potassium-chloride co-
Author NameAffiliation
Henrik StranneheimCenter for Molecular Medicine, Karolinska Institutet
Henrik StranneheimKarolinska University Hospital
Bengt PerssonUppsala University
Bengt PerssonKarolinska Institutet
Bengt PerssonUppsala University
Bengt PerssonKarolinska Institutet
Joakim LundebergRoyal Institute of Technology
Ingrid E SchefferUniversity of Melbourne, Austin Health and Royal Children's Hospital
Ingrid E SchefferFlorey Institute
Maya TopfInstitute of Structural and Molecular Biology, Birkbeck College, University of London
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