The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura (Q24803265)

2

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James Sundholm

3

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John MacMillan

4

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Lyn R Griffiths

https://scigraph.springernature.com/pub.10.1186/1741-7015-2-3

5

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language of work or name

English

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publication date

12 February 2004

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published in

BMC Medicine

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volume

2

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issue

1

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page(s)

3

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exact match

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cites work

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

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Association of the C677T and A1298C polymorphisms in the 5,10 methylenetetrahydrofolate reductase gene in patients with migraine risk

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The homozygous C677T mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for migraine

21 January 2018

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Clinical susceptibility to migraine with aura is modified by dopamine D2 receptor (DRD2) NcoI alleles

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PubMed

https://pubmed.ncbi.nlm.nih.gov/15053827

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1741-7015-2-3

1 reference

Dimensions Publication ID

557039

1020043433

0 references

557039

1 reference

1 reference

1 reference