Copy number and sequence variants implicateAPBA2as an autism candidate gene
Author:
Publisher
Wiley
Subject
Genetics (clinical),Neurology (clinical),General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/aur.107/fullpdf
Reference21 articles.
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2. Novel submicroscopic chromosomal anomalies detected in autism spectrum disorder;Christian;Biological Psychiatry,2008
3. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication;Cook;American Journal of Human Genetics,1997
4. Profiling copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array;de Ståhl;Human Mutation,2008
5. High frequency of neurexin 1B signal peptide structural variants in patients with autism;Feng;Neuroscience Letters,2006
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