(Q48223071)
Statements
1 reference
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. Online (English)
1 reference
1 reference
Martin Dichgans
1 reference
Gisela M Terwindt
1 reference
Michel D Ferrari
1 reference
Kaate R J Vanmolkot
1 reference
Elena Babini
1 reference
Boukje de Vries
1 reference
Anine H Stam
1 reference
Tobias Freilinger
1 reference
Lisa Norris
1 reference
Joost Haan
1 reference
Rune R Frants
1 reference
Nabih M Ramadan
1 reference
Arn M J M van den Maagdenberg
1 reference
1 May 2007
1 reference
1 reference
28
1 reference
5
1 reference
522
1 reference
Identifiers
1 reference
1 reference