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Article

Endophenotypes of FOXP2: dysfunction within the human articulatory network.

European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society - 1 Jul 2011

Liégeois F, Morgan A T, Connelly A, Vargha-Khadem F

Abstract excerpt

The identification of the first gene involved in a speech-language disorder was made possible through the study of a British multi-generational family (the "KE family") in whom half the members have an inherited speech-language disorder caused by a FOXP2 mutation. Neuroimaging investigations in the affected members of the KE family have revealed structural and functional abnormalities in a wide...

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Source

Identifiers

PMID: 21576028
DOI: 10.1016/j.ejpn.2011.04.006

Genes

FOXP2

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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