Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients. [electronic resource]
Producer: 20050503Description: 207-10 p. digitalISSN:- 0387-7604
- Adolescent
- Adult
- Autistic Disorder -- genetics
- Child
- Child, Preschool
- Chromatography, High Pressure Liquid
- Chromosomes, Human, Pair 7 -- genetics
- DNA Mutational Analysis
- DNA Primers
- Female
- Forkhead Transcription Factors
- Humans
- Japan
- Male
- Mutation
- Polymerase Chain Reaction
- Transcription Factors -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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