The prevalence of folate-remedial MTHFR enzyme variants in humans

Studies of rare, inborn metabolic diseases establish that the phenotypes of some mutations in vitamin-dependent enzymes can be suppressed by supplementation of the cognate vitamin, which restores function of the defective enzyme. To determine whether polymorphisms exist that more subtly affect enzym...

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Autors principals: Marini, Nicholas J., Gin, Jennifer, Ziegle, Janet, Keho, Kathryn Hunkapiller, Ginzinger, David, Gilbert, Dennis A., Rine, Jasper
Format: Artigo
Idioma:Inglês
Publicat: National Academy of Sciences 2008
Matèries:
Biological Sciences
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2430358/
https://ncbi.nlm.nih.gov/pubmed/18523009
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0802813105
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