Open AccessNovel SCN1A mutation in the IFMT motif of the α1 subunit of the voltage-gated NaV1.1 channel causing familial hemiplegic migraine
Author(s) -
B De Vries,
CM Weller,
O De Fàbregues,
SC Koelewijn,
AH Stam,
J Haan,
Michel D. Ferrari,
G.M. Terwindt,
AMJ van den Maagdenberg
Publication year - 2013
Publication title -
the journal of headache and pain
Language(s) - English
Resource type - Journals
eISSN - 1129-2377
pISSN - 1129-2369
DOI - 10.1186/1129-2377-1-s1-p19
Subject(s) - medicine , migraine , familial hemiplegic migraine , neurology , genetics , migraine with aura , psychiatry , aura , biology