Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder

BACKGROUND: Autism spectrum disorder (ASD) is an early-onset neurodevelopmental disorder with complex genetic underpinning in its etiology. Copy number variations (CNVs) as one of the genetic factors associated with ASD have been addressed in recent genome-wide association studies (GWAS). However, t...

詳細記述

保存先:
書誌詳細
出版年:Mol Autism
主要な著者: Yin, Chia-Lin, Chen, Hsin-I, Li, Ling-Hui, Chien, Yi-Ling, Liao, Hsiao-Mei, Chou, Miao Chun, Chou, Wen-Jiun, Tsai, Wen-Che, Chiu, Yen-Nan, Wu, Yu-Yu, Lo, Chen-Zen, Wu, Jer-Yuarn, Chen, Yuan-Tsong, Gau, Susan Shur-Fen
フォーマット: Artigo
言語:Inglês
出版事項: BioMed Central 2016
主題:
Research
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4818409/
https://ncbi.nlm.nih.gov/pubmed/27042285
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13229-016-0087-7
タグ: タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!

類似資料