Next-gen sequencing identifies genes associated with speech disorder
A collaborative team of researchers has used next generation sequencing to identify clinically relevant genetic variants associated with a rare pediatric speech disorder. The findings are published in the September 16, 2013 issue of the Journal of Neurodevelopmental Disorders http://www.jneurodevdisorders.com/content/5/1/29. Childhood apraxia of speech (CAS) is a rare, severe speech disorder that in some patients …