Related content

A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2

By Kaunisto M.   Harno H.   Vanmolkot K.   Gargus J.   Sun G.   Hämäläinen E.   Liukkonen E.   Kallela M.   Maagdenberg A.   Frants R.   Färkkilä M.   Palotie A.   Wessman M.  

Neurogenetics, Vol. 5, Iss. 2, 2004-06 ,pp. : 141-146

Springer Publishing Company

Access to resources Recommend Favorite

Functional Effects of Na+,K+-ATPase Gene Mutations Linked to Familial Hemiplegic Migraine

By Capendeguy Oihana   Horisberger Jean-Daniel  

NeuroMolecular Medicine, Vol. 6, Iss. 2-3, 2004-10 ,pp. : 105-116

Humana Press, Inc

Access to resources Recommend Favorite

Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees

By Curtain R. P.   Lea R. A.   Tajouri L.   Haupt L. M.   Ovcaric M.   MacMillan J.   Griffiths L. R.  

Neurological Research, Vol. 27, Iss. 6, 2005-09 ,pp. : 647-652

Maney Publishing

Access to resources Recommend Favorite

A G301R Na⁺/K⁺-ATPase mutation causes familial hemiplegic migraine type 2 with cerebellar signs

By Spadaro Maria   Ursu Simona   Lehmann-Horn Frank   Liana Veneziano   Giovanni Antonini   Paola Giunti   Frontali Marina   Jurkat-Rott Karin  

Neurogenetics, Vol. 5, Iss. 3, 2004-09 ,pp. : 177-185

Springer Publishing Company

Access to resources Recommend Favorite

The genetic features of 24 patients affected by familial and sporadic hemiplegic migraine

By Gallanti A.   Cardin V.   Tonelli A.   Bussone G.   Bresolin N.   Mariani C.   Bassi M.  

Neurological Sciences, Vol. 32, Iss. 1, 2011-05 ,pp. : 141-142

Springer Publishing Company

Access to resources Recommend Favorite