The New England Journal of Medicine
e-mail icon  FREE NEJM E-TOC    HOME   |   SUBSCRIBE   |   CURRENT ISSUE   |   PAST ISSUES   |   COLLECTIONS   |    Advanced Search
Sign in | Get NEJM's E-Mail Table of Contents — Free | Subscribe
 
Correspondence
PreviousPrevious
Volume 356:1680 April 19, 2007 Number 16
NextNext

Long-QT Syndrome

Since this article has no abstract, we have provided an extract of the first 100 words of the full text and any section headings.

 Sign up for free e-toc
 

This Article
-Full Text
- PDF
-PDA Full Text
-Purchase this article

Tools and Services
-Add to Personal Archive
-Add to Citation Manager
-Notify a Friend
-E-mail When Cited
-E-mail When Letters Appear

More Information
-Related Article
 by Imboden, M.
-PubMed Citation
To the Editor: Imboden et al. (Dec. 28 issue)1 report preferential transmission of mutant alleles in the KCNQ1 gene (11p15.5) from mothers to daughters and propose that these mutations confer a selective reproductive advantage. However, allele-specific transmission-ratio distortion2 and grandparental-origin–dependent transmission-ratio distortion3 have been described previously for 11p15.5.2,3 Specifically, the 11p15.5 alleles of a maternal grandmother are more likely (61%) to be transmitted to her granddaughters than to her grandsons.3 The transmission of 11p15.5 alleles that is dependent on their grandparental origin is consistent with these observations.1 Indeed, if females are more likely to be affected, the mutant KCNQ1 alleles . . . [Full Text of this Article]




HOME  |  SUBSCRIBE  |  SEARCH  |  CURRENT ISSUE  |  PAST ISSUES  |  COLLECTIONS  |  PRIVACY  |  HELP  |  beta.nejm.org

Comments and questions? Please contact us.

The New England Journal of Medicine is owned, published, and copyrighted © 2008 Massachusetts Medical Society. All rights reserved.