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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Bibliographic Details
Main Authors:	Goodship, J, Hall, D, Topf, A, Mamasoula, C, Griffin, H, Rahman, T, Glen, E, Tan, H, Palomino Doza, J, Relton, C, Bentham, J, Bhattacharya, S, Cosgrove, C, Brook, D, Granados-Riveron, J, Bu'Lock, F, O'Sullivan, J, Stuart, A, Parsons, J, Cordell, H, Keavney, B
Format:	Journal article
Language:	English
Published:	2012

A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot.

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