The phenotypic manifestations of rare genic CNVs in autism spectrum disorder

The phenotypic manifestations of rare genic CNVs in autism spectrum disorder

Significant evidence exists for the association between copy number variants (CNVs) and Autism Spectrum Disorder (ASD); however, most of this work has focused solely on the diagnosis of ASD. There is limited understanding of the impact of CNVs on the ‘sub-phenotypes' of ASD. The objective of th...

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Bibliographic Details
Main Authors: Merikangas, A K, Segurado, R, Heron, E A, Anney, R J L, Paterson, A D, Cook, E H, Pinto, D, Scherer, S W, Szatmari, P, Gill, M, Corvin, A P, Gallagher, L
Format: Online
Language:English
Published: Nature Publishing Group 2015
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759095/

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https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759095/

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