(Q38861031)

English

Low frequency of mutated methylenetetrahydrofolate reductase 677C-->T and 1298A-->C genetics single nucleotide polymorphisms (SNPs) in Sub-Saharan populations

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Low frequency of mutated methylenetetrahydrofolate reductase 677C-->T and 1298A-->C genetics single nucleotide polymorphisms (SNPs) in Sub-Saharan populations (English)

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

Sub-Saharan Africa

1 reference

based on heuristic

inferred from title

author name string

Charles E Adjalla

1

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Emile K Amouzou

2

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Ambaliou Sanni

3

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Idrissia Abdelmouttaleb

4

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Nicodème W Chabi

5

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Fares Namour

6

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Batoma Soussou

7

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Jean-Louis Guéant

8

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

publication date

1 August 2003

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

Clinical Chemistry and Laboratory Medicine

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Europe PubMed Central

PubMed publication ID

7 September 2017

41

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

1028-1032

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

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

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.158

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.158

21 January 2018

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.158

21 January 2018

The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in whites, Japanese, and Africans

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.158

21 January 2018

Hyperhomocysteinemia is related to residual glomerular filtration and folate, but not to methylenetetrahydrofolate-reductase and methionine synthase polymorphisms, in supplemented end-stage renal disease patients undergoing hemodialysis

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.158

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.158

21 January 2018

Determinants and vitamin responsiveness of intermediate hyperhomocysteinemia (> or = 40 micromol/liter). The Hordaland Homocysteine Study

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.158

21 January 2018

Worldwide distribution of a common methylenetetrahydrofolate reductase mutation

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.158

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2003.158

21 January 2018

Identifiers

10.1515/CCLM.2003.158

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

7 September 2017

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