Human Genetics: The Evolving Story of FOXP2

Fisher, SE

Fisher, SE (reprint author), Max Planck Inst Psycholinguist, Language & Genet Dept, Nijmegen, Netherlands.; Fisher, SE (reprint author), Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands.

CURRENT BIOLOGY, 2019; 29 (2): R65

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 ge......

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