Significant Associations between AXIN1 rs1805105, rs12921862, rs370681 Haplotypes and Variant Genotypes of AXIN2 rs2240308 with Risk of Congenital Heart Defects

This study aimed to investigate possible associations of the susceptibility to congenital heart defects (CHDs) with AXIN1 rs1805105, rs12921862 and rs370681 gene variants and haplotypes, and AXIN2 rs2240308 gene variant. Significant associations were identified for AXIN1 rs370681 and AXIN2 rs2240308...

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Detalles Bibliográficos
Autores principales: Crauciuc, George Andrei, Iancu, Mihaela, Olah, Peter, Tripon, Florin, Anciuc, Mădălina, Gozar, Liliana, Togănel, Rodica, Bănescu, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589771/
https://www.ncbi.nlm.nih.gov/pubmed/33096676
http://dx.doi.org/10.3390/ijerph17207671

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589771/
https://www.ncbi.nlm.nih.gov/pubmed/33096676
http://dx.doi.org/10.3390/ijerph17207671

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