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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Pubblicato in:Oncotarget
Autori principali: Liu, Lin, Wang, Hong-Dan, Cui, Cun-Ying, Qin, Yun-Yun, Fan, Tai-Bing, Peng, Bang-Tian, Zhang, Lian-Zhong, Wang, Cheng-Zeng
Natura: Artigo
Lingua:Inglês
Pubblicazione: Impact Journals LLC 2017
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Research Paper
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5739789/
https://ncbi.nlm.nih.gov/pubmed/29291004
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.22202
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