Rare Copy Number Variations in a Chinese Cohort of Autism Spectrum Disorder

Rare Copy Number Variations in a Chinese Cohort of Autism Spectrum Disorder

Autism spectrum disorder (ASD) is heterogeneous in symptom and etiology. Rare copy number variations (CNVs) are important genetic factors contributing to ASD. Currently chromosomal microarray (CMA) detecting CNVs is recommended as a first-tier diagnostic assay, largely based on research in North Ame...

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Bibliographic Details
Main Authors: Yanjie Fan, Xiujuan Du, Xin Liu, Lili Wang, Fei Li, Yongguo Yu
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-12-01
Series:Frontiers in Genetics
Subjects:
autism spectrum disorder
rare copy number variations
chromosomal microarray
LoF-intolerant genes
RIMS2
Online Access:https://www.frontiersin.org/article/10.3389/fgene.2018.00665/full

Internet

https://www.frontiersin.org/article/10.3389/fgene.2018.00665/full

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