MTRR rs326119 polymorphism is associated with plasma concentrations of homocysteine and cobalamin, but not with congenital heart disease or coronary atherosclerosis in Brazilian patients

BACKGROUND: Differences in the distribution of the MTRR rs326119 polymorphism (c.56 + 781 A > C) between patients with congenital heart disease (CHD) and controls have been described in Chinese individuals. The association is thought to be due to deregulation of homocysteine-cobalamin pathways. T...

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Detalles Bibliográficos
Autores principales: Horita, Melanie, Bueno, Carolina Tosin, Horimoto, Andrea R, Lemos, Pedro A, Morandini-Filho, Antonio A, Krieger, Jose E, Santos, Paulo C J L, Pereira, Alexandre C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454152/
https://www.ncbi.nlm.nih.gov/pubmed/28616555
http://dx.doi.org/10.1016/j.ijcha.2016.11.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454152/
https://www.ncbi.nlm.nih.gov/pubmed/28616555
http://dx.doi.org/10.1016/j.ijcha.2016.11.004

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