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Whole-exome sequencing identifies inherited mutations in autism
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.
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Very interesting.
I
especially liked the jungle test in the fun tests.
- Dan Bierenga
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All fun and informative tests,
I shared them
with all my friends. Great way to better understand folks.
- Matthew McAvoy |
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