Relevance to spina bifida of mutated methylenetetrahydrofolate reductase [33]

Lancet

Volumn 347, Issue 8997, 1996, Pages 340-

  Wilcken, D E L ^a   Wang, X L ^a  

^a Prince Henry Prince of Wales Hosps   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); MUTANT PROTEIN;

ADULT; AGED; FEMALE; HUMAN; LETTER; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SPINA BIFIDA;

EID: 0030034268     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(96)90526-7     Document Type: Letter

References (4)

1. Nm van der Put Rpm Steegers-Theunissen P. Frosst Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida Lancet 346 1995 1070 1071
2. As Whitehead P. Gallagher Jl Mills A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defect Q J Med 88 1995 763 766
3. R. de Franchis G. Sebastio C. Mandato G. Andria P. Mastroiacovo Spina bifida, 677T→C mutation, and role of folate Lancet 346 1995 1703
4. P. Frosst Hj Blom R. Milos A candidate genetic risk-factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase Nature Genet 10 1995 111 113