Annotation Detail
Information
- Associated Genes
- FOXP2
- Associated Variants
-
FOXP2 MUTATION
FOXP2 MUTATION - Associated Disease
- Stuttering, Developmental
- Source Database
- DisGeNET
- Description
- A study of the role of the FOXP2 and CNTNAP2 genes in persistent developmental stuttering.
- Pubmed
- 24807205
- Section of the abstract supporting the evidence
- TITLE
- Number of the section of the abstract supporting the evidence
- 0
- Number of the sentence supporting the evidence
- 0
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
Drugs