Whole-exome sequencing revealed novel genetic alterations in patients with tetralogy of Fallot

BACKGROUND: The most prevalent cyanotic congenital heart disease (CHD) phenotype is tetralogy of Fallot (TOF). Rare genetic variations have been identified as significant risk factors for CHD. Thus, this research sought to identify the pathogenic variations and molecular etiologies of TOF. METHODS:...

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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 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644019/
https://www.ncbi.nlm.nih.gov/pubmed/37969115
http://dx.doi.org/10.21037/tp-23-449

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644019/
https://www.ncbi.nlm.nih.gov/pubmed/37969115
http://dx.doi.org/10.21037/tp-23-449

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