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Article

A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering.

Neurobiology of disease - 1 Sept 2014

Han Tae-Un, Park John, Domingues Carlos F, Moretti-Ferreira Danilo, Paris Emily, Sainz Eduardo, Gutierrez Joanne, Drayna Dennis

Abstract excerpt

A number of speech disorders including stuttering have been shown to have important genetic contributions, as indicated by high heritability estimates from twin and other studies. We studied the potential contribution to stuttering from variants in the FOXP2 gene, which have previously been assoc...

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Identifiers

PMID: 24807205
DOI: 10.1016/j.nbd.2014.04.019
PMCID: PMC4099264

Genes

CNTNAP2
FOXP2
GNPTAB
GNPTG
NAGPA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24807205-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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