Abnormal folate metabolism and genetic polymorphism of the folate pathway in a child with Down syndrome and neural tube defect. [electronic resource]
Producer: 20011025Description: 128-32 p. digitalISSN:- 0148-7299
- Amino Acids, Sulfur -- blood
- Consanguinity
- DNA -- genetics
- DNA Methylation
- Down Syndrome -- enzymology
- Folic Acid -- metabolism
- Genotype
- Humans
- Infant
- Male
- Methylenetetrahydrofolate Reductase (NADPH2)
- Mutation
- Neural Tube Defects -- enzymology
- Oxidoreductases Acting on CH-NH Group Donors -- genetics
- Polymorphism, Genetic
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Publication Type: Case Reports; Journal Article
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