Methyltetrahydrofolate reductase C677T gene mutation and hyperhomocysteinemia as a novel risk factor for diabetic nephropathy

Endocrine

Volumn 36, Issue 2, 2009, Pages 255-261

  Ukinc, Kubilay ^a   Ersoz, Halil Onder ^b   Karahan, Caner ^b   Erem, Cihangir ^b   Eminagaoglu, Selcuk ^b   Hacihasanoglu, Arif Bayram ^b   Yilmaz, Mustafa ^b   Kocak, Mustafa ^b  

^a ÇANAKKALE ONSEKIZ MART UNIVERSITY   (Turkey)

^b KARADENIZ TECHNICAL UNIVERSITY   (Turkey)

Author keywords

Diabetic nephropathy; Hyperhomocysteinemia; MTHFR C677T mutation; Type 2 diabetes

Indexed keywords

HOMOCYSTEINE; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);

ADULT; ARTICLE; BLOOD; DIABETIC NEPHROPATHY; DIABETIC NEUROPATHY; DISEASE PREDISPOSITION; FEMALE; GENE FREQUENCY; GENETICS; GENOTYPE; HUMAN; HYPERHOMOCYSTEINEMIA; MALE; MIDDLE AGED; NON INSULIN DEPENDENT DIABETES MELLITUS; PHYSIOLOGY; POINT MUTATION; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; DIABETES MELLITUS, TYPE 2; DIABETIC NEPHROPATHIES; DIABETIC NEUROPATHIES; DISEASE SUSCEPTIBILITY; FEMALE; GENE FREQUENCY; GENOTYPE; HOMOCYSTEINE; HUMANS; HYPERHOMOCYSTEINEMIA; MALE; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); MIDDLE AGED; POINT MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS;

EID: 73349125452     PISSN: 1355008X     EISSN: 15590100     Source Type: Journal    
DOI: 10.1007/s12020-009-9218-7     Document Type: Article

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