(Q43760550)

26 November 2017

title

Genetic defects as important factors for moderate hyperhomocysteinemia (English)

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26 November 2017

J Geisel

1

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26 November 2017

I Zimbelmann

2

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26 November 2017

H Schorr

3

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26 November 2017

J P Knapp

4

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26 November 2017

M Bodis

5

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26 November 2017

U Hübner

6

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26 November 2017

W Herrmann

7

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26 November 2017

publication date

1 August 2001

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Clinical Chemistry and Laboratory Medicine

26 November 2017

published in

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26 November 2017

volume

39

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26 November 2017

issue

8

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26 November 2017

page(s)

698-704

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

26 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.115

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/10.1515%2FCCLM.2001.115

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.115

World distribution of the T833C/844INS68 CBS in cis double mutation: a reliable anthropological marker

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.115

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.115

Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.115

A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.115

Role of homocysteine, cystathionine and methylmalonic acid measurement for diagnosis of vitamin deficiency in high-aged subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.115

Elevation of 2-methylcitric acid I and II levels in serum, urine, and cerebrospinal fluid of patients with cobalamin deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.115

Thermolabile variant of 5,10-methylenetetrahydrofolate reductase associated with low red-cell folates: implications for folate intake recommendations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.115

Molecular genetics of homocysteine metabolism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FCCLM.2001.115

21 January 2018

Identifiers

DOI

10.1515/CCLM.2001.115

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26 November 2017

1 reference