Endophenotypes of FOXP2: Dysfunction within the human articulatory network

European Journal of Paediatric Neurology

Volumn 15, Issue 4, 2011, Pages 283-288

  Liegeois F ^a   Morgan, A T ^b   Connelly, A ^c   Vargha Khadem, F ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b MURDOCH CHILDREN'S RESEARCH INSTITUTE   (Australia)

^c FLOREY INSTITUTE OF NEUROSCIENCE AND MENTAL HEALTH   (Australia)

Author keywords

Articulation; Developmental verbal dyspraxia; fMRI; FOXP2

Indexed keywords

TRANSCRIPTION FACTOR FOXP2;

BASAL GANGLION; CASE REPORT; CEREBELLUM; CONFERENCE PAPER; CONTROLLED STUDY; ELECTROENCEPHALOGRAM; ENDOPHENOTYPE; FEMALE; FUNCTIONAL MAGNETIC RESONANCE IMAGING; HUMAN; IMITATION; LINGUISTICS; MALE; NERVE CELL NETWORK; PREMOTOR CORTEX; PRIMARY MOTOR CORTEX; PRIORITY JOURNAL; SPEECH DISORDER; SUPPLEMENTARY MOTOR AREA;

ADULT; BASAL GANGLIA; BRAIN; CEREBELLAR DISEASES; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LANGUAGE DEVELOPMENT DISORDERS; MALE; MOTOR CORTEX; NERVE NET; PHENOTYPE; SEVERITY OF ILLNESS INDEX; SPEECH;

EID: 79958801139     PISSN: 10903798     EISSN: 15322130     Source Type: Journal    
DOI: 10.1016/j.ejpn.2011.04.006     Document Type: Conference Paper

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