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

Erstveröffentlichung

2016

Authors

Fan, Chunxiang

Wolking, Stefan

Lehmann-Horn, Frank

Hedrich, Ulrike B. S.

Freilinger, Tobias

et al.

Wissenschaftlicher Artikel

Published in

Cephalalgia ; 36 (2016), 13. - S. 1238-1247. - ISSN 0333-1024. - eISSN 1468-2982

Link to publication

https://dx.doi.org/10.1177/0333102415608360

Institutions

UKU. Klinik für Neurologie
Neurophysiologie
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

Metadata

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