Novel SCN1A mutation in the IFMT motif of the α1 subunit of the voltage-gated NaV1.1 channel causing familial hemiplegic migraine.

Authors :: De Vries, B
Weller, CM
De Fàbregues, O
Koelewijn, SC
Stam, AH
Haan, J
Ferrari, MD
Terwindt, GM
van den Maagdenberg, AMJ
Source :: Journal of Headache & Pain; Feb2013 Supplement, Vol. 14, p1-1, 1p
Publication Year :: 2013
Abstract: An abstract of the article "Novel SCN1A mutation in the IFMT motif of the Α1 subunit of the voltage-gated NaV1.1 channel causing familial hemiplegic migraine" by B. De Vries, C. M. Weller, O. De Fàbregues, S. C. Koelewijn, A. H. Stam and colleagues is presented.

Subjects :: GENES
HEMIPLEGIA
INTERVIEWING
CASE studies
GENETIC mutation
MIGRAINE
DISEASE complications
GENETICS

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