Title : Methylenetetrahydrofolate reductase C677T mutation, plasma homocysteine, and folate in subjects from northern Italy with or without angiographically documented severe coronary atherosclerotic disease: evidence for an important genetic-environmental interaction.

Pub. Date : 1998 Jun 1

PMID : 9596662






2 Functional Relationships(s)
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Compound Name
Protein Name
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1 A point mutation (C677T; Ala-to-Val) in the gene encoding the 5, 10-methylenetetrahydrofolate reductase (MTHFR) has been recently reported to render the enzyme thermolabile and less active. Alanine methylenetetrahydrofolate reductase Homo sapiens
2 A point mutation (C677T; Ala-to-Val) in the gene encoding the 5, 10-methylenetetrahydrofolate reductase (MTHFR) has been recently reported to render the enzyme thermolabile and less active. Alanine methylenetetrahydrofolate reductase Homo sapiens