CNVs leading to fusion transcripts in individuals with autism spectrum disorder

CNVs leading to fusion transcripts in individuals with autism spectrum disorder

عرض إصدارات أخرى (1)

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′...

وصف كامل

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Holt, R, Sykes, N, Conceição, I, Cazier, J, Anney, R, Oliveira, G, Gallagher, L, Vicente, A, Monaco, A, Pagnamenta, A
التنسيق: Journal article
اللغة:English
منشور في: 2012

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