Home » Psychology news » Whole-exome sequencing identifies inherited mutations in autism

Whole-exome sequencing identifies inherited mutations in autism

January 23, 2013 by

While autism clearly runs in some families, few inherited genetic causes have been found. A major reason is that these causes are so varied that it's hard to find enough people with a given mutation to establish a clear pattern. Researchers have now pinpointed several inherited mutations -- among the first to be identified -- through an unusual approach: Using whole-exome sequencing to study large Middle Eastern families with autism.

Leave a Reply

Your email address will not be published. Required fields are marked *

*

You may use these HTML tags and attributes: <a href="" title=""> <abbr title=""> <acronym title=""> <b> <blockquote cite=""> <cite> <code> <del datetime=""> <em> <i> <q cite=""> <strike> <strong>