Novel Genetic Variants of Sporadic Atrial Septal Defect (ASD) in a Chinese Population Identified by Whole-Exome Sequencing (WES)

BACKGROUND: Recently, mutations in several genes have been described to be associated with sporadic ASD, but some genetic variants remain to be identified. The aim of this study was to use whole-exome sequencing (WES) combined with bioinformatics analysis to identify novel genetic variants in cases...

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Detalles Bibliográficos
Autores principales: Liu, Yong, Cao, Yu, Li, Yaxiong, Lei, Dongyun, Li, Lin, Hou, Zong Liu, Han, Shen, Meng, Mingyao, Shi, Jianlin, Zhang, Yayong, Wang, Yi, Niu, Zhaoyi, Xie, Yanhua, Xiao, Benshan, Wang, Yuanfei, Li, Xiao, Yang, Lirong, Wang, Wenju, Jiang, Lihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2018
Materias:
Clinical Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849354/
https://www.ncbi.nlm.nih.gov/pubmed/29505555
http://dx.doi.org/10.12659/MSM.908923

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5849354/
https://www.ncbi.nlm.nih.gov/pubmed/29505555
http://dx.doi.org/10.12659/MSM.908923

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