CNVs leading to fusion transcripts in individuals with autism spectrum disorder

There is strong evidence that rare copy number variants (CNVs) have a role in susceptibility to autism spectrum disorders (ASDs). Much research has focused on how CNVs mediate a phenotypic effect by altering gene expression levels. We investigated an alternative mechanism whereby CNVs combine the 5′...

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主要な著者:	Holt, R, Sykes, N, Conceição, I, Cazier, J, Anney, R, Oliveira, G, Gallagher, L, Vicente, A, Monaco, A, Pagnamenta, A
フォーマット:	Journal article
言語:	English
出版事項:	2012

CNVs leading to fusion transcripts in individuals with autism spectrum disorder. 著者: Holt, R, Sykes, N, Conceição, I, Cazier, J, Anney, R, Oliveira, G, Oliveira, G, Gallagher, L, Vicente, A, Monaco, A, Pagnamenta, A

出版事項 2012

Journal article

CNVs leading to fusion transcripts in individuals with autism spectrum disorder

CNVs leading to fusion transcripts in individuals with autism spectrum disorder. 著者: Holt, R, Sykes, N, Conceição, I, Cazier, J, Anney, R, Oliveira, G, Oliveira, G, Gallagher, L, Vicente, A, Monaco, A, Pagnamenta, A

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