A genetic understanding of language development through cognitive and neurogenetic studies: an exploration of the FOXP2 gene, songbird development, human language, and autism
It is well known that FOXP2 has a connection to human language. In a familial case study of humans in one family with a mutated FOXP2, it was found that all members showed Developmental Verbal Dyspraxia, a cognitive language deficit. In knock out experiments in mice, it was found that FOXP2 is cr...
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| Language: | en_US |
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The University of Arizona.
2017
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| Online Access: | http://hdl.handle.net/10150/626743 http://arizona.openrepository.com/arizona/handle/10150/626743 |