FOXP2 and the neuroanatomy of speech and language

2005/02/01 by Faraneh Vargha-Khadem, Faraneh Vargha‐Khadem, David G. Gadian +3 · 1 citation
Biochemistry, Genetics and Molecular Biology · Neuroscience · Psychology · #Biology #Cognitive science #Congenital heart defects research #DECIPHER #FOXP2 #Function (biology) #Gene #Genetics #Language Development and Disorders #Linguistics #Mutation #Neuroanatomy #Neuroscience #Psychology #TRACE (psycholinguistics) #Williams Syndrome Research

paper · doi:10.1038/nrn1605

crossref issued 2005/02/01 · crossref published 2005/02/01 · crossref published-print 2005/02/01 · openalex publication_date 2005/02/01 · crossref created 2005/02/01 · crossref deposited 2024/01/21 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/29 · crossref indexed 2026/08/06

Citations

• A forkhead-domain gene is mutated in a severe speech and language disorder
• Basal ganglia and cerebellar loops: motor and cognitive circuits
• ParallelFoxP1andFoxP2Expression in Songbird and Human Brain Predicts Functional Interaction
• Sequential Organization of Multiple Movements: Involvement of Cortical Motor Areas
• Evaluation of the role of phonological STM in the development of vocabulary in children: A longitudinal study

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