Deep exon resequencing of DLGAP2 as a candidate gene of autism spectrum disorders

BACKGROUND: 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 t...

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Detalhes bibliográficos
Main Authors: Chien, Wei-Hsien, Gau, Susan Shur-Fen, Liao, Hsiao-Mei, Chiu, Yen-Nan, Wu, Yu-Yu, Huang, Yu-Shu, Tsai, Wen-Che, Tsai, Ho-Min, Chen, Chia-Hsiang
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3751063/
https://ncbi.nlm.nih.gov/pubmed/23915500
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2040-2392-4-26
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