Abstract
Complex diseases are far more common than diseases that follow simple Mendelian patterns of inheritance. Difficulties are experienced in the designing of experiments to dissect out the contribution of a single allele to a complex phenotype. We review the literature regarding a point mutation in methylenetetrahydrofolate reductase, a candidate gene for susceptibility to vascular diseases.
Publication types
-
Research Support, Non-U.S. Gov't
-
Review
MeSH terms
-
Alleles
-
Arteriosclerosis / blood
-
Arteriosclerosis / genetics*
-
Databases, Bibliographic
-
Folic Acid / blood
-
Genetic Predisposition to Disease
-
Homocysteine / blood
-
Homozygote
-
Humans
-
MEDLINE
-
Methylenetetrahydrofolate Reductase (NADPH2)
-
Oxidoreductases Acting on CH-NH Group Donors / genetics*
-
Point Mutation*
Substances
-
Homocysteine
-
Folic Acid
-
Oxidoreductases Acting on CH-NH Group Donors
-
Methylenetetrahydrofolate Reductase (NADPH2)