Functionally Significant, Rare Transcription Factor Variants in Tetralogy of Fallot

OBJECTIVE: 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 cardiac outflow tract...

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Detalles Bibliográficos
Autores principales: Töpf, Ana, Griffin, Helen R., Glen, Elise, Soemedi, Rachel, Brown, Danielle L., Hall, Darroch, Rahman, Thahira J., Eloranta, Jyrki J., Jüngst, Christoph, Stuart, A. Graham, O'Sullivan, John, Keavney, Bernard D., Goodship, Judith A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122343/
https://www.ncbi.nlm.nih.gov/pubmed/25093829
http://dx.doi.org/10.1371/journal.pone.0095453

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122343/
https://www.ncbi.nlm.nih.gov/pubmed/25093829
http://dx.doi.org/10.1371/journal.pone.0095453

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