Whole exome sequencing identifies novel inherited genetic variants in tetralogy of Fallot

BACKGROUND: Tetralogy of Fallot (TOF) is the most common neonatal cyanotic heart defect, and genetic variation is an important risk factor for the etiology of TOF. Identifying TOF-associated genetic variants is critical to understanding susceptibility and outcome in patients with TOF and may help de...

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Detalles Bibliográficos
Autores principales: Pan, Yu, Liu, Manli, Zhang, Songsong, Mei, Huaxian, Wu, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442507/
https://www.ncbi.nlm.nih.gov/pubmed/36071769
http://dx.doi.org/10.21037/jtd-22-970

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9442507/
https://www.ncbi.nlm.nih.gov/pubmed/36071769
http://dx.doi.org/10.21037/jtd-22-970

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