Connection of GLI1 variants to congenital heart disease susceptibility: A case-control study

The purpose of this study was to investigate the relationship between glioma-associated oncogene homolog 1 (GLI1) rs2228226 and rs10783826 polymorphisms and congenital heart disease (CHD) risk in a Chinese Han population. Genotyping for our interested polymorphisms was performed using polymerase cha...

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Detalles Bibliográficos
Autores principales: Guan, Weiwei, Zhang, Jun, Chen, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2020
Materias:
3400
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337459/
https://www.ncbi.nlm.nih.gov/pubmed/32629623
http://dx.doi.org/10.1097/MD.0000000000019868

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7337459/
https://www.ncbi.nlm.nih.gov/pubmed/32629623
http://dx.doi.org/10.1097/MD.0000000000019868

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