Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine-Reference-Cited by-同舟云学术

Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine

Published:2007-10-19 Issue:12 Volume:52 Page:990-998
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Castro Maria-José,Stam Anine H.,Lemos Carolina,Barros José,Gouveia Raquel G.,Martins Isabel Pavão,Koenderink Jan B.,Vanmolkot Kaate R. J.,Mendes Alexandre P.,Frants Rune R.,Ferrari Michel D.,Sequeiros Jorge,Pereira-Monteiro José M.,van den Maagdenberg Arn M. J. M.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/jhg2007131.pdf

Reference32 articles.

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3. Bassi MT, Bresolin N, Tonelli A, Nazos K, Crippa F, Baschirotto C, Zucca C, Bersano A, Dolcetta D, Boneschi FM, Barone V, Casari G (2004) A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood. J Med Genet 41:621–628

4. Battistini S, Stenirri S, Piatti M, Gelfi C, Righetti PG, Rocchi R, Giannini F, Battistini N, Guazzi GC, Ferrari M, Carrera P (1999) A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia. Neurology 53:38–43

5. Capendeguy O, Horisberger JD (2004) Functional effects of Na+,K+-ATPase gene mutations. Neuromol Med 6:105–116

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