NOTCH2, ATIC, MRI1, SLC6A13, ATP13A2 Genetic Variations are Associated with Ventricular Septal Defect in the Chinese Tibetan Population Through Whole-Exome Sequencing

BACKGROUND: Ventricular septal defect (VSD) is the most common congenital cardiac abnormality in children and the second most common in adults. This study aimed to explore the potentially causative genes in VSD patients in the Chinese Tibetan population, and to provide a theoretical basis for the ge...

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Detalles Bibliográficos
Autores principales: Zhang, Xiaohui, Zhen, Da, Li, Xuemei, Yi, Faling, Zhang, Zhanhao, Yang, Wei, Li, Xuguang, Sheng, Yemeng, Liu, Xiaoli, Jin, Tianbo, He, Yongjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10150769/
https://www.ncbi.nlm.nih.gov/pubmed/37138656
http://dx.doi.org/10.2147/PGPM.S404438

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10150769/
https://www.ncbi.nlm.nih.gov/pubmed/37138656
http://dx.doi.org/10.2147/PGPM.S404438

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