(Q28201142)

1

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F. M. Salzano

2

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J. L. Rupert

3

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M. H. Hutz

4

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K. Hill

5

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A. M. Hurtado

6

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P. W. Hochachka

7

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D. V. Devine

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

8

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language of work or name

English

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publication date

July 2003

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published in

Annals of Human Genetics

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volume

67

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issue

Pt 4

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4

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page(s)

367-71

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367-371

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cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1469-1809.2003.00027.X

Alu insertions versus blood group plus protein genetic variability in four Amerindian populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1469-1809.2003.00027.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1469-1809.2003.00027.X

Altitude as a risk factor for congenital anomalies

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1469-1809.2003.00027.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1469-1809.2003.00027.X

The methylfolate axis in neural tube defects: in vitro characterisation and clinical investigation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1469-1809.2003.00027.X

Heterogeneity in world distribution of the thermolabile C677T mutation in 5,10-methylenetetrahydrofolate reductase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1469-1809.2003.00027.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1469-1809.2003.00027.X

Worldwide distribution of a common methylenetetrahydrofolate reductase mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1469-1809.2003.00027.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1469-1809.2003.00027.X

Mutation A1298C of methylenetetrahydrofolate reductase: risk for early coronary disease not associated with hyperhomocysteinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1469-1809.2003.00027.X

Role of thrombin in pulmonary fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1469-1809.2003.00027.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1469-1809.2003.00027.X

A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1469-1809.2003.00027.X