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Atrial Septal Defects Caused By Endocardial Specific Deficiency Of Transcription Factor Tbx5

Mona Nemer,Mathieu Nadeau,Romain Georges,Brigitte Laforest,Chantal Lefebvre,Gregor Andelfinger,Benoit Bruneau,Pierre Paradis

Circulation（2007）

Cited 23|Views16
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Abstract
In human, mutations in transcription factor Tbx5 cause the Holt Oram syndrome (HOS) characterized by forelimb and a large spectrum of cardiac malformations ranging from simple arrhythmia to complex...
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Key words
transcription factor tbx5,atrial septal defects,endocardial specific deficiency
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