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  Human genetics: The evolving story of FOXP2

Fisher, S. E. (2019). Human genetics: The evolving story of FOXP2. Current Biology, 29(2), R65-R67. doi:10.1016/j.cub.2018.11.047.

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Item Permalink: https://hdl.handle.net/21.11116/0000-0002-CEBE-1 Version Permalink: https://hdl.handle.net/21.11116/0000-0002-CEC5-8
Genre: Journal Article

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Fisher__2019_Human genetics.pdf (Publisher version), 316KB
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 Creators:
Fisher, Simon E.1, 2, Author           
Affiliations:
1Language and Genetics Department, MPI for Psycholinguistics, Max Planck Society, ou_792549              
2Donders Institute for Brain, Cognition and Behaviour, External Organizations, ou_55236              

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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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Language(s): eng - English
 Dates: 2018-122019-01-212019-01
 Publication Status: Issued
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 Rev. Type: Peer
 Identifiers: DOI: 10.1016/j.cub.2018.11.047
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Title: Current Biology
  Other : Curr. Biol.
Source Genre: Journal
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Publ. Info: London, UK : Cell Press
Pages: - Volume / Issue: 29 (2) Sequence Number: - Start / End Page: R65 - R67 Identifier: ISSN: 0960-9822
CoNE: https://pure.mpg.de/cone/journals/resource/954925579107