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- Title
Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease.
- Authors
Junker, R; Kotthoff, S; Vielhaber, H; Halimeh, S; Kosch, A; Koch, H G; Kassenböhmer, R; Heineking, B; Nowak-Göttl, U
- Abstract
Recently, an association between the homozygous C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in infants with congenital neural tube defects or congenital oral clefts has been shown. However, no data are available so far with respect to the MTHFR 677TT genotype in children with underlying structural congenital heart disease (CHD).
- Publication
Cardiovascular research, 2001, Vol 51, Issue 2, p251
- ISSN
0008-6363
- Publication type
Journal Article
- DOI
10.1016/s0008-6363(01)00286-3