Breakthrough gene correct technique could repair disease-causing mutation

August 3, 2017, 8:14 AM|
Scientists in a U.S. have successfully remade a inadequate gene in tellurian embryos for a initial time. Researchers used a absolute record famous as CRISPR to repair a DNA turn that causes an hereditary form of heart disease. Seventy-two percent of a ensuing embryos were disease-free. Dr. David Agus joins “CBS This Morning” to plead the intensity and reliable concerns.

Short URL:

Posted by on Aug 3 2017. Filed under Health & Medicine. You can follow any responses to this entry through the RSS 2.0. You can leave a response or trackback to this entry

Leave a Reply

Photo Gallery

Log in | Designed by hitechnews