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Whole-exome sequencing identifies inherited mutations in autism
January 23, 2013 by NewsBot
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.