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A1298C methylenetetrahydrofolate reductase mutation and coronary artery disease: relationships with C677T polymorphism and homocysteine/folate metabolism.
Friso, S; Girelli, D; Trabetti, E; Stranieri, C; Olivieri, O; Tinazzi, E; Martinelli, N; Faccini, G; Pignatti, P F; Corrocher, R.
Affiliation
  • Friso S; Department of Clinical and Experimental Medicine, University of Verona, Italy.
Clin Exp Med ; 2(1): 7-12, 2002 May.
Article in En | MEDLINE | ID: mdl-12049191
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Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Genetic / Coronary Artery Disease / Folic Acid / Oxidoreductases Acting on CH-NH Group Donors / Homocysteine Type of study: Etiology_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Clin Exp Med Journal subject: MEDICINA Year: 2002 Document type: Article Affiliation country: Country of publication:
Search on Google
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Polymorphism, Genetic / Coronary Artery Disease / Folic Acid / Oxidoreductases Acting on CH-NH Group Donors / Homocysteine Type of study: Etiology_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Clin Exp Med Journal subject: MEDICINA Year: 2002 Document type: Article Affiliation country: Country of publication: