MTHFR 677C→T mutation and neural-tube defects [7]

Lancet

Volumn 350, Issue 9089, 1997, Pages 1479-1480

  Rizzari, C ^a   Valsecchi, M G ^a   Conter, V ^a  

^a UNIVERSITY OF MILAN   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); FOLIC ACID; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); OXIDOREDUCTASE;

DIETARY INTAKE; GENE FREQUENCY; GENE MUTATION; GENOTYPE; HUMAN; LETTER; NEURAL TUBE DEFECT; PRIORITY JOURNAL; RACE DIFFERENCE; GENETICS; MUTATION; NOTE; RISK FACTOR;

FOLIC ACID; GENE FREQUENCY; HUMANS; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); MUTATION; NEURAL TUBE DEFECTS; OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS; RISK FACTORS;

EID: 0031583644     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(05)64248-1     Document Type: Letter

References (5)

1. DE Wilcken MTHFR 677C→T mutation, folate intake, neural-tube defect, and risk of cardiovascular disease Lancet 350 1997 603 604
2. R De Franchis G Sebastio C Mandata Spina bifida, 677C→T mutation, and role of folate Lancet 346 1995 173
3. A Tosetto E Missiaglia M Frezzato The VITA project: C677T mutation in the methylene-tetrahydrofolate reductase gene and risk of venous thromboembolism Br J Haematol 97 1997 804 806
4. E Grandone M Margaglione D Colaizzo Factor V Leiden, C>T MTHFR polymorphism and genetic susceptibility to preeclampsia Thromb Haemost 77 1997 1052 1054
5. E Sacchi L Tagliabue F Duca High frequency of the C677T mutation in the methylene-tetrahydrofolate reductase (MTHFR) gene in northern Italy Thromb Haemost 78 1997 963 964