Is mutated serine hydroxymethyltransferase (SHMT) involved in the etiology of neural tube defects? [electronic resource]
Producer: 20010830Description: 164-72 p. digitalISSN:- 1096-7192
- Adolescent
- Adult
- Alleles
- Base Sequence
- Child
- Cytosol -- enzymology
- DNA Mutational Analysis
- DNA, Complementary -- chemistry
- Female
- Folic Acid -- blood
- Genotype
- Glycine Hydroxymethyltransferase -- genetics
- Humans
- Mitochondria -- enzymology
- Mutation
- Neural Tube Defects -- enzymology
- Polymorphism, Genetic
- Polymorphism, Single-Stranded Conformational
- Sequence Deletion
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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