Case Reports
Journal Article
Add like
Add dislike
Add to saved papers

A new episodic ataxia syndrome with linkage to chromosome 19q13.

BACKGROUND: Multiple episodic ataxia phenotypes and genotypes have been described.

OBJECTIVE: To describe a new episodic ataxia syndrome.

DESIGN: Genomewide linkage analysis with dense single nucleotide polymorphism arrays.

SETTING: University clinic. Patients Family with lifelong episodes of ataxia and normal interictal examination results.

RESULTS: Suggestive linkage (logarithm of odds score, 3.27) to a 10-centimorgan region on chromosome 19q13.

CONCLUSION: A new dominantly inherited episodic ataxia syndrome is linked to chromosome 19q.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app