Links between genetics and pathophysiology in the autism spectrum disorders
Author:
Affiliation:
1. The Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK
Publisher
EMBO
Subject
Molecular Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/emmm.201100157
Reference114 articles.
1. Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene
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3. WHOLE BLOOD SEROTONIN IN AUTISTIC AND NORMAL SUBJECTS
4. A genome-wide scan for common alleles affecting risk for autism
5. A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism
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