Haploinsufficiency of АТР1А2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2 (Nat. Genet. — 2003. — FEB. — 33(2). — P. 192—196: англ.)

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Abstract

The prevalence of migraine in Western countries shows 12% of the entire population. One of the hereditary forms of the disease is familial hemiplegic migraine of the second type, which clinically manifests an aura, paroxysm of headache and the development of transient hemiparesis during an attack.

About the authors

M. De. Fusco

Dibit-San Raffaele Scientific Institute

Author for correspondence.
Email: info@eco-vector.com

Human Molecular Genetics Unit

Italy, Milan

R. Marconi

Dibit-San Raffaele Scientific Institute

Email: info@eco-vector.com

Human Molecular Genetics Unit

Italy, Milan

L. Silvestri

Dibit-San Raffaele Scientific Institute

Email: info@eco-vector.com

Human Molecular Genetics Unit

Italy, Milan

L. Atorino

Dibit-San Raffaele Scientific Institute

Email: info@eco-vector.com

Human Molecular Genetics Unit

Italy, Milan

L. Rampoldi

Dibit-San Raffaele Scientific Institute

Email: info@eco-vector.com

Human Molecular Genetics Unit

Italy, Milan

L. Morgante

Dibit-San Raffaele Scientific Institute

Email: info@eco-vector.com

Human Molecular Genetics Unit

Italy, Milan

A. Ballabio

Dibit-San Raffaele Scientific Institute

Email: info@eco-vector.com

Human Molecular Genetics Unit

Italy, Milan

P. Aridon

Dibit-San Raffaele Scientific Institute

Email: info@eco-vector.com

Human Molecular Genetics Unit

Italy, Milan

G. Casari

Dibit-San Raffaele Scientific Institute

Email: info@eco-vector.com

Human Molecular Genetics Unit

Italy, Milan

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Copyright (c) 2003 Fusco M.D., Marconi R., Silvestri L., Atorino L., Rampoldi L., Morgante L., Ballabio A., Aridon P., Casari G.

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