Endophenotypes of FOXP2: dysfunction within the human articulatory network. [electronic resource]
Producer: 20120507Description: 283-8 p. digitalISSN:- 1532-2130
- Adult
- Basal Ganglia -- physiopathology
- Brain -- physiopathology
- Cerebellar Diseases -- genetics
- Female
- Forkhead Transcription Factors -- deficiency
- Genetic Predisposition to Disease -- genetics
- Humans
- Language Development Disorders -- diagnosis
- Male
- Motor Cortex -- physiopathology
- Nerve Net -- physiopathology
- Phenotype
- Severity of Illness Index
- Speech -- physiology
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Publication Type: Journal Article
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