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Epigenomic and Transcriptomic Dynamics During Human Heart Organogenesis

RATIONALE -: There is growing evidence that common variants and rare sequence alterations in regulatory sequences can result in birth defects or predisposition to disease. Congenital heart defects (CHDs) are the most common birth defect and have a clear genetic component, yet only a third of cases c...

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Detalhes bibliográficos
Publicado no:Circ Res
Main Authors: VanOudenhove, Jennifer, Yankee, Tara N., Wilderman, Andrea, Cotney, Justin
Formato: Artigo
Idioma:Inglês
Publicado em: 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7554226/
https://ncbi.nlm.nih.gov/pubmed/32772801
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCRESAHA.120.316704
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