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22q11.2 Deletion Status and Disease Burden in Children and Adolescents with Tetralogy of Fallot
BACKGROUND: Patients with repaired tetralogy of Fallot (TOF) experience variable outcomes for reasons that are incompletely understood. We hypothesize that genetic variants contribute to this variability. We sought to investigate the association of 22q11.2 deletion status with clinical outcome in pa...
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| Pubblicato in: | Circ Cardiovasc Genet |
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| Autori principali: | , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4383312/ https://ncbi.nlm.nih.gov/pubmed/25561045 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.114.000819 |
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