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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Detaylı Bibliyografya
Yayımlandı:Circ Cardiovasc Genet
Asıl Yazarlar: Mercer-Rosa, Laura, Paridon, Stephen M., Fogel, Mark A., Rychik, Jack, Tanel, Ronn E., Zhao, Huaqing, Zhang, Xuemei, Yang, Wei, Shults, Justine, Goldmuntz, Elizabeth
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2015
Konular:
Article
Online Erişim: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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