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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Detalles Bibliográficos
Autores principales: Fan, Yanjie, Du, Xiujuan, Liu, Xin, Wang, Lili, Li, Fei, Yu, Yongguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305546/
https://www.ncbi.nlm.nih.gov/pubmed/30619482
http://dx.doi.org/10.3389/fgene.2018.00665

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305546/
https://www.ncbi.nlm.nih.gov/pubmed/30619482
http://dx.doi.org/10.3389/fgene.2018.00665

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