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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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| Publicado no: | Medicine (Baltimore) |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wolters Kluwer Health
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7337459/ https://ncbi.nlm.nih.gov/pubmed/32629623 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000019868 |
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