Whole exome sequencing identifies novel mutation in eight Chinese children with isolated tetralogy of Fallot

BACKGROUND: Tetralogy of Fallot is the most common cyanotic congenital heart disease. However, its pathogenesis remains to be clarified. The purpose of this study was to identify the genetic variants in Tetralogy of Fallot by whole exome sequencing. METHODS: Whole exome sequencing was performed amon...

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Detalles Bibliográficos
Autores principales: Liu, Lin, Wang, Hong-Dan, Cui, Cun-Ying, Qin, Yun-Yun, Fan, Tai-Bing, Peng, Bang-Tian, Zhang, Lian-Zhong, Wang, Cheng-Zeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739789/
https://www.ncbi.nlm.nih.gov/pubmed/29291004
http://dx.doi.org/10.18632/oncotarget.22202

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739789/
https://www.ncbi.nlm.nih.gov/pubmed/29291004
http://dx.doi.org/10.18632/oncotarget.22202

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