A novel missense ATP1A2 mutation in a Finnish family with familial hemiplegic migraine type 2-Reference-Cited by-同舟云学术

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

Published:2004-05-07 Issue:2 Volume:5 Page:141-146
ISSN:1364-6745
Container-title:Neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

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

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10048-004-0178-z.pdf

Cited by 55 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Astrocytes in Atp1a2 ‐deficient heterozygous mice exhibit hyperactivity after induction of cortical spreading depression;FEBS Open Bio;2020-04-23

2. Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families;Neuron;2018-05

3. The contribution of CACNA1A, ATP1A2 and SCN1A mutations in hemiplegic migraine: A clinical and genetic study in Finnish migraine families;Cephalalgia;2018-02-27

4. Common variant burden contributes significantly to the familial aggregation of migraine in 1,589 families;2017-11-30

5. Recurrent coma and fever in familial hemiplegic migraine type 2. A prospective 15-year follow-up of a large family with a novel ATP1A2 mutation;Cephalalgia;2016-05-24

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