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

ABSTRACT: 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 associated with developmental verbal dyspraxia, and from variants in the CNTNAP2 gene, which have been associated with specific language impairment (SLI). DNA sequence analysis of these two genes in a group of 602 unrelated cases, all with familial persistent developmental stuttering, revealed no excess of potentially deleterious coding sequence variants in the cases compared to a matched group of 487 well characterized neurologically normal controls. This was compared to the distribution of variants in

SUBMITTER: Han TU 

PROVIDER: S-EPMC4099264 | biostudies-literature | 2014 Sep

REPOSITORIES: biostudies-literature