MTHFR C677T and A1298C variants in Mexican Mestizo infants with neural tube defects from Western Mexico-Reference-Cited by-同舟云学术

MTHFR C677T and A1298C variants in Mexican Mestizo infants with neural tube defects from Western Mexico

Published:2021-05-29 Issue:5 Volume:61 Page:188-192
ISSN:0914-3505
Container-title:Congenital Anomalies
language:en
Short-container-title:Congenit Anom

Author:

Aranda‐Sánchez Cristian Irela¹,Bobadilla‐Morales Lucina¹²,Corona‐Rivera Alfredo¹²,Cuero‐Quezada Idalid²,Santana‐Hernández Jennifer²,Baldomero‐López Alejandra¹,Romero‐Bolaño Yaneris M.¹,Peña‐Padilla Christian¹,Corona‐Rivera Jorge Román¹²^ORCID

Affiliation:

1. Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, “Dr. Juan I. Menchaca” Civil Hospital of Guadalajara Guadalajara Mexico

2. “Dr. Enrique Corona‐Rivera” Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center University of Guadalajara Guadalajara Mexico

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cga.12429

Reference10 articles.

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2. A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects;Whitehead AS;QJM,1995

3. Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD)

4. Prevalence of open neural tube defects and risk factors related to isolated anencephaly and spina bifida in live births from the “Dr. Juan I. Menchaca” Civil Hospital of Guadalajara (Jalisco, Mexico)

5. Methylenetetrahydrofolate reductase and spina bifida: Evaluation of level of defect and maternal genotypic risk in Hispanics

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2. Polimorfismo de proteína 5,10-metilentetrahidrofolato reductasa en población venezolana;Revista Digital de Postgrado;2023-07-24

3. Abnormal methylation caused by folic acid deficiency in neural tube defects;Open Life Sciences;2022-01-01