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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Shranjeno v:
Bibliografske podrobnosti
izdano v:Front Genet
Main Authors: Fan, Yanjie, Du, Xiujuan, Liu, Xin, Wang, Lili, Li, Fei, Yu, Yongguo
Format: Artigo
Jezik:Inglês
Izdano: Frontiers Media S.A. 2018
Teme:
Genetics
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6305546/
https://ncbi.nlm.nih.gov/pubmed/30619482
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2018.00665
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