Early-onset familial hemiplegic migraine due to a novel SCN1A mutation

Erstveröffentlichung
2016Authors
Fan, Chunxiang
Wolking, Stefan
Lehmann-Horn, Frank
Hedrich, Ulrike B. S.
Freilinger, Tobias
Wissenschaftlicher Artikel
Published in
Cephalalgia ; 36 (2016), 13. - S. 1238-1247. - ISSN 0333-1024. - eISSN 1468-2982
Link to publication
https://dx.doi.org/10.1177/0333102415608360Institutions
UKU. Klinik für NeurologieNeurophysiologie
UKU. Institut für Humangenetik
Subject headings
[Free subject headings]: Familial hemiplegic migraine | early-onset | gain of function | FHM3 | Na(V)1 | 1 | severe myoclonic epilepsy | sodium-channel | gabaergic interneurons | mouse model | seizures | phenotype | genetics | defects | infancy | type-1[DDC subject group]: DDC 610 / Medicine & health