Two novel SCNIA mutations identified in families with familial hemiplegic migraine

Author(s):
Weller, C.M.; Pelzer, N.; Vries, B. de; Lopez, M.A.; Fabregues, O. de; Pascual, J.; Arroyo, M.A.R.; Koelewijn, S.C.; Stam, A.H.; Haan, J.; Ferrari, M.D. (0000-0001-9691-9449); Terwindt, G.M.; Maagdenberg, A.M.J.M. van den (0000-0002-9310-5535)
Published
2014
Publication type
Article / Letter to editor
Migraineion channel defectsfamilial hemiplegic migraineSCNIA gene
Date issued
2014-11-30
Language
English
Is part of
Cephalalgia (2014), Vol. 34, no. 13, p. 1062-1069
hdl
1887/100564
doi
10.1177/0333102414529195