Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
Original research article by G. Carvil et al. (2013).
Read the article here.
The researchers used genetic sequence analysis to study a group of 65 genes known to cause epilepsy. They found that changes in the CHD2 gene were related to health and behavior differences like autism spectrum disorder and epilepsy.