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Article

The role of candidate-gene CNTNAP2 in childhood apraxia of speech and specific language impairment.

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics - 1 Oct 2015

Centanni T M, Sanmann J N, Green J R, Iuzzini-Seigel J, Bartlett C, Sanger W G, Hogan T P

Abstract excerpt

Childhood apraxia of speech (CAS) is a debilitating pediatric speech disorder characterized by varying symptom profiles, comorbid deficits, and limited response to intervention. Specific Language Impairment (SLI) is an inherited pediatric language disorder characterized by delayed and/or disorder...

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Source

Identifiers

PMID: 26097074
DOI: 10.1002/ajmg.b.32325

Genes

CNTNAP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-26097074-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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