Association of MTR gene polymorphisms with the occurrence of non-syndromic congenital heart disease: a case–control study

To exhaustively explore the association of infant genetic polymorphisms of methionine synthase (MTR) gene with the risk of non-syndromic congenital heart disease (CHD). A hospital-based case–control study involving 620 CHD cases and 620 health controls was conducted from November 2017 to March 2020....

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Detalles Bibliográficos
Autores principales: Liu, Yiping, Zhong, Taowei, Song, Xinli, Zhang, Senmao, Sun, Mengting, Wei, Jianhui, Shu, Jing, Yang, Tubao, Wang, Tingting, Qin, Jiabi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10256807/
https://www.ncbi.nlm.nih.gov/pubmed/37296303
http://dx.doi.org/10.1038/s41598-023-36330-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10256807/
https://www.ncbi.nlm.nih.gov/pubmed/37296303
http://dx.doi.org/10.1038/s41598-023-36330-x

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