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Volumn 28, Issue 7-8, 2009, Pages 809-812

The methylenetetrahydrofolate reductase gene variant (C677T) as a susceptibility gene for tetralogy of Fallot

Author keywords

Genetic polymorphism; Methylenetetrahydrofolate reductase; Tetralogy of Fallot

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); GENOMIC DNA;

EID: 70350319243     PISSN: 08702551     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (17)

References (11)
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    • A candidate genetic risk factor for vascular disease: A common mutation in methyleneletrahydrofolate reductase
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    • Frosst, P.1
  • 5
    • 0037384215 scopus 로고    scopus 로고
    • 5,10-Methylenetetrahydrofolate reductase 677C - >T and 1298A - >C mutations are genetic determinants of elevated homocysteine
    • Castro, R. et al., 5,10-Methylenetetrahydrofolate reductase 677C - >T and 1298A - >C mutations are genetic determinants of elevated homocysteine. QJMed, 2003; 96(4): 297-303.
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    • Castro, R.1
  • 6
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    • Maternal MTHFR 677C>T is a risk factor for congenital heart defects: Effect modification by periconceptional folate supplementation
    • van Beynum, I.M. et al., Maternal MTHFR 677C>T is a risk factor for congenital heart defects: effect modification by periconceptional folate supplementation. Eur Heart J, 2006; 27(8): 981-987
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  • 8
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    • Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases
    • Lee, C.N. et al., Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases. Acta Obstet Gynecol Scand, 2005; 84(12): 1134-1140
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  • 9
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    • Lack of evidence of association between MTHFR C677T polymorphism and congenital heart disease in a TDT study design
    • Pereira, A.C. et al., Lack of evidence of association between MTHFR C677T polymorphism and congenital heart disease in a TDT study design. Int J Cardiol, 2005; 105(1): 15-18
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.