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′...

Disgrifiad llawn

Manylion Llyfryddiaeth
Prif Awduron:	Holt, R, Sykes, N, Conceição, I, Cazier, J, Anney, R, Oliveira, G, Gallagher, L, Vicente, A, Monaco, A, Pagnamenta, A
Fformat:	Journal article
Iaith:	English
Cyhoeddwyd:	2012

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

Cyhoeddwyd 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. gan 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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