Genetics: Rare epilepsy syndromes share autism mutations

Individuals with either of two rare forms of epilepsy have duplications or deletions that encompass genes implicated in autism and language impairment, according to a study published 27 June in Epilepsia1.

Read more…

This entry was posted in Home-News, Press Room. Bookmark the permalink. Comments are closed, but you can leave a trackback: Trackback URL.