Annotation Detail
Information
- Associated Genes
- FOXP2
- Associated Variants
-
FOXP2 MUTATION
FOXP2 MUTATION - Associated Disease
- Apraxia, Developmental Verbal
- Source Database
- DisGeNET
- Description
- 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).
- Pubmed
- 24807205
- Section of the abstract supporting the evidence
- ALL_TEXT_1/3
- Number of the section of the abstract supporting the evidence
- 1
- Number of the sentence supporting the evidence
- 2
- Original source reporting the Gene Disease association
- BeFree,CLINVAR,CTD_human,ORPHANET,UNIPROT
- DisGENET score for the Gene Disease association
- 0.483800186209124
Drugs