Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders
Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders
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Publisher
England: BioMed Central Ltd
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Language
English
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Publisher
England: BioMed Central Ltd
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Contents
We recently reported a terminal deletion of approximately 2.4 Mb at chromosome 8p23.2-pter in a boy with autism. The deleted region contained the DLGAP2 gene that encodes the neuronal post-synaptic density protein, discs, large (Drosophila) homolog-associated protein 2. The study aimed to investigate whether DLGAP2 is genetically associated with au...
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Full title
Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3751063
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3751063
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ISSN
2040-2392
E-ISSN
2040-2392
DOI
10.1186/2040-2392-4-26
