CORDIS Project
Funding breakdown and partner intelligence are Premium
Sign in and upgrade to Premium for EU contribution totals, consortium analytics, OpenAlex research context, and AI summaries. · 0 consortium intelligence fields visible of 1
Start free • Cancel anytime • 14-day refund guarantee
This project investigates the genetic basis of language disorders by studying the FOXP2 gene and its effects on neuronal function. It aims to understand how mutations in this gene impact speech and language development.
The identification of genomic variants associated with common neurodevelopmental syndromes is rapidly advancing.
Recent estimates suggest that hundreds of genes are likely to contribute to susceptibility to a specific syndrome.
Inherent in this hypothesis is the convergence of associated variants on common molecular networks mediating specific endophenotypes such as disturbed speech and language development across clinically distinct categories.
Highly penetrant mutations account for only a frac…
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE
Partner organizations (coordinator is shown above), with normalized type and CORDIS activity type. Guests see up to 4 partners.
Similar projects, consortium collaboration history, frequent partners, and OpenAlex research context.
Guests see up to 5 EuroSciVoc fields.
Guests see up to 5 topics.
