Genetic Variants of ISL1 Gene Promoter Identified from Congenital Tetralogy of Fallot Patients Alter Cellular Function Forming Disease Basis

Tetralogy of Fallot (TOF) is the most common cyanotic congenital heart disease in newborns. ISL1 is a master transcription factor in second heart field development, whereas the roles of ISL1 gene promoter variants in TOF patients have not been genetically investigated. Total DNA extraction from 601...

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Detalles Bibliográficos
Autores principales: Yin, Xiu-Yun, Chen, Huan-Xin, Chen, Zhuo, Yang, Qin, Han, Jun, He, Guo-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953631/
https://www.ncbi.nlm.nih.gov/pubmed/36830727
http://dx.doi.org/10.3390/biom13020358

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953631/
https://www.ncbi.nlm.nih.gov/pubmed/36830727
http://dx.doi.org/10.3390/biom13020358

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