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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 |
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| Autori principali: | , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Impact Journals LLC
2017
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| Soggetti: | |
| 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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