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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Opis bibliograficzny
Główni autorzy:	Holt, R, Sykes, N, Conceição, I, Cazier, J, Anney, R, Oliveira, G, Gallagher, L, Vicente, A, Monaco, A, Pagnamenta, A
Format:	Journal article
Język:	English
Wydane:	2012

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

Wydane 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. od 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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