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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Oncotarget
Egile Nagusiak: Liu, Lin, Wang, Hong-Dan, Cui, Cun-Ying, Qin, Yun-Yun, Fan, Tai-Bing, Peng, Bang-Tian, Zhang, Lian-Zhong, Wang, Cheng-Zeng
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Impact Journals LLC 2017
Gaiak:
Research Paper
Sarrera elektronikoa: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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