Functionally significant, rare transcription factor variants in tetralogy of Fallot.

Functionally significant, rare transcription factor variants in tetralogy of Fallot.

<h4>Objective</h4>Rare variants in certain transcription factors involved in cardiac development cause Mendelian forms of congenital heart disease. The purpose of this study was to systematically assess the frequency of rare transcription factor variants in sporadic patients with the car...

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Main Authors: Ana Töpf, Helen R Griffin, Elise Glen, Rachel Soemedi, Danielle L Brown, Darroch Hall, Thahira J Rahman, Jyrki J Eloranta, Christoph Jüngst, A Graham Stuart, John O'Sullivan, Bernard D Keavney, Judith A Goodship
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0095453
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https://doi.org/10.1371/journal.pone.0095453

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