Methylenetetrahydrofolate reductase (MTHFR): incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifida (Q73301011)

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scientific article published on May 15, 2003

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English	Methylenetetrahydrofolate reductase (MTHFR): incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifida	scientific article published on May 15, 2003

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scholarly article

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2 November 2019

Methylenetetrahydrofolate reductase (MTHFR): incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifida (English)

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2 November 2019

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26 December 2023

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Decio Brunoni

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2 November 2019

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Ana Beatriz Alvarez Perez

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2 November 2019

Vânia D'Almeida

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2 November 2019

Naja Vergani

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2 November 2019

Fernanda Teresa de Lima

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2 November 2019

Allan C. de Oliveira

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1 May 2003

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2 November 2019

15 May 2003

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26 December 2023

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https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.10059

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26 December 2023

American Journal of Medical Genetics

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2 November 2019

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2 November 2019

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2 November 2019

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2 November 2019

5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review

1 reference

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21 January 2018

Prevalence of the mutation C677 --> T in the methylene tetrahydrofolate reductase gene among distinct ethnic groups in Brazil

2

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Epidemiology of neural tube defects in South America

5

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Metabolic effects of C677T and A1298C mutations at the MTHFR gene in Brazilian children with neural tube defects

7

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Prevention of the First Occurrence of Neural-Tube Defects by Periconceptional Vitamin Supplementation

8

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The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy

9

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Folates and the fetus

11

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A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

13

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Role of the C677T polymorphism at the MTHFR gene on risk to nonsyndromic cleft lip with/without cleft palate: results from a case-control study in Brazil

14

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Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

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Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency

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Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations

17

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Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida population

19

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A simple salting out procedure for extracting DNA from human nucleated cells

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Homocysteine metabolism in pregnancies complicated by neural-tube defects

21

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Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects

22

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Methylenetetrahydrofolate reductase and neural tube defects

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Methylenetetrahydrofolate reductase (MTHFR): the incidence of mutations C677T and A1298C in the Ashkenazi Jewish population

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Homocysteine metabolism

27

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The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.

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Possible interaction of genotypes at cystathionine β-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects

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

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Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

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A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

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A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects

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10.1002/AJMG.A.10059

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12707953%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12707953%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

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