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Article

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.

European journal of human genetics : EJHG - 1 Oct 2009

Vernes Sonja C, MacDermot Kay D, Monaco Anthony P, Fisher Simon E

Abstract excerpt

Neurodevelopmental disorders that disturb speech and language are highly heritable. Isolation of the underlying genetic risk factors has been hampered by complexity of the phenotype and potentially large number of contributing genes. One exception is the identification of rare heterozygous mutations of the FOXP2 gene in a monogenic syndrome characterised by impaired sequencing of articulatory gestures, disrupting...

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Source

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Identifiers

PMID: 19352412
DOI: 10.1038/ejhg.2009.43
PMCID: PMC2784575

Genes

FOXP1
FOXP2

Provenance

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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