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

B. de Vries,Claudia M. Weller,O. de Fàbregues,Stephany C. Koelewijn,Anine H. Stam,Joost Haan,Ferrari,Gisela M. Terwindt,Amj van den Maagdenberg

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

2013

B. de Vries
Claudia M. Weller
O. de Fàbregues
Stephany C. Koelewijn
Anine H. Stam
Joost Haan
Ferrari
Gisela M. Terwindt
Amj van den Maagdenberg

Familial hemiplegic migraine (FHM) is a monogenic subtype of migraine with aura. So far three FHM genes are identified; the CACNA1A gene, the ATP1A2 gene and the SCN1A gene.

Keywords:

Anesthesia
Migraine
Mutation Carrier
Genetics
Neuroscience
Familial hemiplegic migraine
NAV1
Migraine with aura
Gene
Medicine
Mutation
ATP1A2
scn1a mutation
Voltage-gated ion channel
α1 subunit

Correction
Source
Cite
Save
Machine Reading By IdeaReader

References

Citations