Familial basilar migraine associated with a new mutation in the ATP1A2 gene

[en] Basilar migraine (BM), familial hemiplegic migraine (FHM), and sporadic hemiplegic migraine (SHM) are phenotypically similar subtypes of migraine with aura, differentiated only by motor symptoms, which are absent in BM. Mutations in CACNA1A and ATP1A2 have been found in FHM. The authors detected a novel mutation in the ATP1A2 gene (R548H) in members of a family with BM, suggesting that BM and FHM may be allelic disorders.

Disciplines :

Neurology

Author, co-author :

Ambrosini, A.

D'Onofrio, M.

Grieco, G. S.

Di Mambro, A.

Montagna, G.

Fortini, D.

Nicoletti, F.

Nappi, G.

Sances, G.

Schoenen, Jean ; Université de Liège - ULiège > Département des sciences biomédicales et précliniques > Neuro-anatomie

More authors (3 more)

Language :

English

Title :

Familial basilar migraine associated with a new mutation in the ATP1A2 gene

Publication date :

13 December 2005

Journal title :

Neurology

ISSN :

0028-3878

eISSN :

1526-632X

Publisher :

Lippincott Williams & Wilkins, Philadelphia, United States - Pennsylvania

Volume :

Issue :

Pages :

1826-1828

Peer reviewed :

Peer Reviewed verified by ORBi

Available on ORBi :

since 25 September 2009

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Bibliography

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