Mutations in genes related to myocyte contraction and ventricular septum development in non-syndromic tetralogy of Fallot

OBJECTIVE: Eighty percent of patients with a diagnosis of tetralogy of Fallot (TOF) do not have a known genetic etiology or syndrome. We sought to identify key molecular pathways and biological processes that are enriched in non-syndromic TOF, the most common form of cyanotic congenital heart diseas...

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Detalles Bibliográficos
Autores principales: Harvey, Drayton C., Verma, Riya, Sedaghat, Brandon, Hjelm, Brooke E., Morton, Sarah U., Seidman, Jon G., Kumar, S. Ram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569225/
https://www.ncbi.nlm.nih.gov/pubmed/37840956
http://dx.doi.org/10.3389/fcvm.2023.1249605

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10569225/
https://www.ncbi.nlm.nih.gov/pubmed/37840956
http://dx.doi.org/10.3389/fcvm.2023.1249605

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