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Volumn 9, Issue 4, 2000, Pages 205-207

Genetic polymorphism of methylenetetrahydrofolate reductase (MTHFR) and coronary artery disease

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); HOMOCYSTEINE;

EID: 0033758293     PISSN: 10611711     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01623895     Document Type: Article
Times cited : (1)

References (17)
  • 1
    • 0007379818 scopus 로고
    • A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase: Isolation of cDNA, mapping and mutation identification
    • (1995) Nat Genet , vol.17 , pp. 195-200
    • Frosst, P.1    Blom, H.J.2    Milos, R.3
  • 7
    • 0029655527 scopus 로고    scopus 로고
    • Nutritional ecogenetic: Homocysteine-related arteriosclerotic vascular disease, neural tube defects and folic acid
    • (1996) Am J Hurn Genetic , vol.58 , pp. 17-20
    • Motulsky, A.G.1
  • 15
    • 0032941872 scopus 로고    scopus 로고
    • The TT genotype of methylenetetrahydrofolate reductase C 677 T gene polymorphism is associated with the extent of coronary atherosclerosis in patients at high risk for coronary artery disease
    • (1999) Eur Hear J , vol.20 , pp. 584-592
    • Gardemann, A.1    Wiedemann, H.2    Philipp, M.3
  • 17
    • 0033013119 scopus 로고    scopus 로고
    • Hyperhomocysteinemia in high-aged subjects: Relation of B-vitamins, folic acid, renal function and the methylenetetrahydrofolate reductase mutation
    • (1999) Atherosclerosis , vol.144 , pp. 91-101
    • Herrmann, W.1    Quast, S.2    Ullrich, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.