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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Bibliografiske detaljer
Main Authors:	Holt, R, Sykes, N, Conceição, I, Cazier, J, Anney, R, Oliveira, G, Gallagher, L, Vicente, A, Monaco, A, Pagnamenta, A
Format:	Journal article
Sprog:	English
Udgivet:	2012

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

Udgivet 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. af 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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