A Common Variant in the PTPN11 Gene Contributes to the Risk of Tetralogy of Fallot

BACKGROUND: Tetralogy of Fallot (TOF) is the commonest cyanotic form of congenital heart disease. In 80% of cases, TOF behaves as a complex genetic condition exhibiting significant heritability. As yet, no common genetic variants influencing TOF risk have been robustly identified. METHODS AND RESULT...

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Опубликовано в: :Circ Cardiovasc Genet
Главные авторы: Goodship, Judith A., Hall, Darroch, Topf, Ana, Mamasoula, Chrysovalanto, Griffin, Helen, Rahman, Thahira J., Glen, Elise, Tan, Huay, Doza, Julian Palomino, Relton, Caroline L., Bentham, Jamie, Bhattacharya, Shoumo, Cosgrove, Catherine, Brook, David, Granados-Riveron, Javier, Bu’Lock, Frances A., O’Sullivan, John, Stuart, A. Graham, Parsons, Jonathan, Cordell, Heather J., Keavney, Bernard
Формат: Artigo
Язык:Inglês
Опубликовано: 2012
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4643453/
https://ncbi.nlm.nih.gov/pubmed/22503907
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.111.962035
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