Mutation C677T of methylenetetrahydrofolate reductase gene is not associated with coronary artery disease, but possibly with albuminuria, in type 2 diabetic patients.

Wirta, V; Huang, X H; Wirta, O; Rantalaiho, V; Pasternack, A; Jokela, H; Koivula, T; Lehtimäki, T

Wirta, V; Huang, X H; Wirta, O; Rantalaiho, V; Pasternack, A; Jokela, H; Koivula, T; Lehtimäki, T.

Affiliation

Wirta V; Department of Medical Biochemistry, University of Tampere Medical School, Finland.

Clin Chem Lab Med ; 36(8): 625-8, 1998 Aug.

Article in En | MEDLINE | ID: mdl-9806473

Subject(s)

Albuminuria/genetics; Coronary Disease/genetics; Diabetes Mellitus, Type 2/genetics; Mutation; Oxidoreductases Acting on CH-NH Group Donors/genetics; Adult; Aged; Albuminuria/complications; Albuminuria/enzymology; Coronary Disease/complications; Coronary Disease/enzymology; Diabetes Mellitus, Type 2/complications; Diabetes Mellitus, Type 2/enzymology; Humans; Methylenetetrahydrofolate Reductase (NADPH2); Middle Aged

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Coronary Disease / Diabetes Mellitus, Type 2 / Albuminuria / Oxidoreductases Acting on CH-NH Group Donors / Mutation Type of study: Risk_factors_studies Limits: Adult / Aged / Humans / Middle aged Language: En Journal: Clin Chem Lab Med Journal subject: QUIMICA CLINICA / TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 1998 Document type: Article Affiliation country: Finland Country of publication: Germany

Search on Google

Add to My VHL

XML

PubMed Links