Early-onset familial hemiplegic migraine due to a novel SCN1A mutation.
Cephalalgia
; 36(13): 1238-1247, 2016 Nov.
Article
in En
| MEDLINE
| ID: mdl-26763045
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Genetic Testing
/
Genetic Predisposition to Disease
/
Migraine with Aura
/
Polymorphism, Single Nucleotide
/
NAV1.1 Voltage-Gated Sodium Channel
Type of study:
Prognostic_studies
Limits:
Adult
/
Child
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Cephalalgia
Year:
2016
Type:
Article
Affiliation country:
Germany