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Volumn 57, Issue 3, 2000, Pages 230-231
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Spina bifida and common mutations at the homocysteine metabolism pathway
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Author keywords
[No Author keywords available]
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Indexed keywords
5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2);
CYSTATHIONINE BETA SYNTHASE;
FOLIC ACID;
HOMOCYSTEINE;
METHIONINE SYNTHASE;
AMINO ACID METABOLISM;
CONTROLLED STUDY;
ENZYME DEFICIENCY;
GENE MUTATION;
HUMAN;
LETTER;
MAJOR CLINICAL STUDY;
MATERNAL NUTRITION;
MULTIFACTORIAL GENETIC DISORDER;
NEURAL TUBE DEFECT;
PRIORITY JOURNAL;
SPINA BIFIDA;
SUPPLEMENTATION;
5-METHYLTETRAHYDROFOLATE-HOMOCYSTEINE S-METHYLTRANSFERASE;
ALLELES;
CASE-CONTROL STUDIES;
CYSTATHIONINE BETA-SYNTHASE;
FEMALE;
GENOTYPE;
HOMOCYSTEINE;
HUMANS;
METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);
MOTHERS;
MUTATION;
OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS;
RISK;
SPINAL DYSRAPHISM;
VITAMIN B 12;
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EID: 0034068966
PISSN: 00099163
EISSN: None
Source Type: Journal
DOI: 10.1034/j.1399-0004.2000.570310.x Document Type: Letter |
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Times cited : (17)
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References (0)
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