☆ 4.1 Article

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

NEUROGENETICS (2004)

Get Full Text
Add to Collection

Journal

NEUROGENETICS
Volume 5, Issue 2, Pages 141-146

Publisher

SPRINGER
DOI: 10.1007/s10048-004-0178-z

Keywords

familial hemiplegic migraine; linkage; DNA sequence analysis; Na+-K+-exchanging ATPase; missense mutation

Categories

Genetics & Heredity Clinical Neurology

Funding

  1. NIMH NIH HHS [R01 MH59222] Funding Source: Medline
  2. NINDS NIH HHS [R01 NS37675-02] Funding Source: Medline

Ask authors/readers for more resources

Protocol

Community support

Reagent

Community support

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.1
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available
Webinars Posters Questions Hubs Funding Journals Papers Connect Collections Reviewers About Us FAQs Mobile App Privacy Policy Terms of Use
© Peeref 2019-2024. All rights reserved.