Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot

PURPOSE: To determine disease-associated single-gene variants in conotruncal defects, particularly tetralogy of Fallot (TOF). METHODS: We analyzed for rare loss-of-function and deleterious variants in FLT4 (VEGFR3) and other genes in the vascular endothelial growth factor (VEGF) pathway, as part of...

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Detalles Bibliográficos
Autores principales: Reuter, Miriam S., Jobling, Rebekah, Chaturvedi, Rajiv R., Manshaei, Roozbeh, Costain, Gregory, Heung, Tracy, Curtis, Meredith, Hosseini, S. Mohsen, Liston, Eriskay, Lowther, Chelsea, Oechslin, Erwin, Sticht, Heinrich, Thiruvahindrapuram, Bhooma, Mil, Spencer van, Wald, Rachel M., Walker, Susan, Marshall, Christian R., Silversides, Candice K., Scherer, Stephen W., Kim, Raymond H., Bassett, Anne S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2018
Materias:
Brief Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752294/
https://www.ncbi.nlm.nih.gov/pubmed/30232381
http://dx.doi.org/10.1038/s41436-018-0260-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752294/
https://www.ncbi.nlm.nih.gov/pubmed/30232381
http://dx.doi.org/10.1038/s41436-018-0260-9

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