Influencia del polimorfismo rs1801133 y concentraciones de homocisteína en la susceptibilidad a defectos congénitos folato-sensibles

Introduction: Multiple polymorphic variants of the Methylenetetrahydrofolate reductase gene associated with folate-sensitive birth defects have been described; the rs1801133 polymorphism is considered as the most frequent genetic cause of hyperhomocysteinemia. Objective: To relate maternal plasma ho...

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Bibliographic Details

Main Authors:	Taboada Lugo, Noel, Herrera Martínez, Manuela, Ferreira Capote, Raúl Pablo, Concepción Álvarez, Alina, Machín Parapar, Elizabeth, Collazo Mesa, Teresa
Format:	Article
Language:	Spanish
Published:	2025
Subjects:	Defectos Congénitos Deficiencia de Ácido Fólico Polimorfismo Genético Hipermocisteinemia Congenital abnormalities folic acid deficiency polymorphism genetic hyperhomocysteinemia
Online Access:	https://dialnet.unirioja.es/servlet/oaiart?codigo=10296208
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