MicroRNAs as the cause of schizophrenia in 22q11.2 deletion carriers, and possible implications for idiopathic disease: a mini-review

The 22q11.2 deletion is the strongest known genetic risk factor for schizophrenia. Research has implicated microRNA-mediated dysregulation in 22q11.2 deletion syndrome (22q11.2DS) schizophrenia risk. Primary candidate genes are DGCR8, which encodes a component of the microprocessor complex essential...

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出版年:	Frontiers in Molecular Neuroscience
主要な著者:	Andreas J. eForstner, Franziska eDegenhardt, Gerhard eSchratt, Markus M. eNöthen
フォーマット:	論文
言語:	英語
出版事項:	Frontiers Media S.A. 2013-12-01
主題:	Schizophrenia microRNA DGCR8 22q11.2 deletion syndrome MIR185 copy number variants
オンライン･アクセス:	http://journal.frontiersin.org/Journal/10.3389/fnmol.2013.00047/full