Spontaneous mutations in the brain gene TBR1 disrupt the function of the encoded protein in children with severe autism. In addition, there is a direct link between TBR1 and FOXP2, a well-known ...
Spontaneous mutations in the brain gene TBR1 disrupt the function of the encoded protein in children with severe autism. In addition, there is a direct link between TBR1 and FOXP2, a well-known ...
Spontaneous mutations in the brain gene TBR1 disrupt the function of the encoded protein in children with severe autism. These are the main findings of Pelagia Deriziotis and colleagues at the ...
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