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-  2019 

Human Genetics: The Evolving Story of FOXP2

DOI: https://doi.org/10.1016/j.cub.2018.11.047

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Abstract:

FOXP2 mutations cause a speech and language disorder, raising interest in potential roles of this gene in human evolution. A new study re-evaluates genomic variation at the human FOXP2 locus but finds no evidence of recent adaptive evolution

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