Parental Genetic Variants, MTHFR 677C>T and MTRR 66A>G, Associated Differently with Fetal Congenital Heart Defect

BACKGROUND: Congenital heart defect (CHD) is one of the most common birth defects in the world. The methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) genes are two of the most important candidate genes for fetal CHD. However, the correlations between the two genes...

Descripción completa

Detalles Bibliográficos
Autores principales: Guo, Qian-nan, Wang, Hong-dan, Tie, Li-zhen, Li, Tao, Xiao, Hai, Long, Jian-gang, Liao, Shi-xiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512027/
https://www.ncbi.nlm.nih.gov/pubmed/28758112
http://dx.doi.org/10.1155/2017/3043476

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5512027/
https://www.ncbi.nlm.nih.gov/pubmed/28758112
http://dx.doi.org/10.1155/2017/3043476

Ejemplares similares