Maternal MTHFR genotype and haplotype predict deficits in early cognitive development in a lead-exposed birth cohort in Mexico City
Author(s) -
J. Richard Pilsner,
Howard Hu,
Robert O. Wright,
Katarzyna Kordas,
Adrienne S. Ettinger,
Brisa N. Sánchez,
David E. Cantonwine,
Alicia Lazarus,
Alejandra Cantoral,
Lourdes Schnaas,
Martha María TéllezRojo,
Mauricio HernándezÁvila
Publication year - 2010
Publication title -
american journal of clinical nutrition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.608
H-Index - 336
eISSN - 1938-3207
pISSN - 0002-9165
DOI - 10.3945/ajcn.2009.28839
Subject(s) - methylenetetrahydrofolate reductase , genotype , medicine , pregnancy , haplotype , cohort , offspring , allele , genetics , biology , gene
Maternal folate nutritional status and prenatal lead exposure can influence fetal development and subsequent health. The methylenetetrahydrofolate reductase (MTHFR) gene is important for folate metabolism, and 2 common polymorphisms, C677T and A1298C, reduce enzymatic activity; C677T is present at high penetrance in Mexican populations.
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