NIH Research Matters—Congenital heart disease genomics

From NIH Research Matters: Clues to Congenital Heart Disease A large-scale genomic analysis found that non-inherited mutations in hundreds of genes together account for about 1 in 10 cases of severe congenital heart defects, the most common type of birth defect.     Editor's Picks from past issues: Hormone May Help Treat Diabetes Gene Linked to Migraine and Sleep Disorder Red Meat-Heart Disease Link Involves Gut Microbes Gut Microbes Affect Weight After Gastric Bypass Killing Cancer With Radioactive Bacteria NIH Research Matters is on Facebook! Join us at www.facebook.com/ResearchMatters, and write on our wall. NIH Research Matters is also available as an RSS News Feed. Point your RSS reader to http://www.nih.gov/researchmatters/feed.xml (to learn more about RSS, visit http://www.nih.gov/news/rss.htm).   Update Your E-mail Address | Add Subscriptions | Unsubscribe If you have questions or problems with the subscription service, please contact support@govdelivery.com. For all other inquiries about NIH programs and activities, please contact NIHinfo@od.nih.gov. Before writing, please view our Frequently Asked Questions page, our A-Z Health Topics page, or Search our website. This service is provided to you by the National Institutes of Health. NIH…Turning Discovery Into Health® This email was sent to kostikblog@ukr.net using GovDelivery, on behalf of: National Institutes of Health (NIH) · 9000 Rockville Pike · Bethesda MD 20892 · 301-496-4000 / TTY 301-402-9612