A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation.

De Cunto, Angela

A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation. [electronic resource] - Pediatric neurology Aug 2012 - 133-6 p. digital

Publication Type: Case Reports; Journal Article

1873-5150

10.1016/j.pediatrneurol.2012.04.012 doi


Amino Acid Sequence
Child, Preschool
Humans
Male
Migraine with Aura--diagnosis
Molecular Sequence Data
Mutation--genetics
Pedigree
Sodium-Potassium-Exchanging ATPase--genetics