MTHFR gene polymorphisms analyzed in population from Kolkata, West Bengal [2]

Indian Journal of Human Genetics

Volumn 13, Issue 1, 2007, Pages 38-

  Mukhopadhyay, K ^a   Dutta, S ^a   Das Bhomik, A ^a  

^a Manovikas Biomedical Research and Diagnostic Centre   (India)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2);

CARDIOVASCULAR DISEASE; DNA METHYLATION; DNA POLYMORPHISM; DNA SYNTHESIS; ENZYME ACTIVITY; ETHNIC AND RACIAL GROUPS; GENE; GENETIC POLYMORPHISM; HUMAN; HYPERHOMOCYSTEINEMIA; LETTER; MORBIDITY; MORTALITY; MTHFR GENE; POPULATION GENETICS;

EID: 34247877737     PISSN: 09716866     EISSN: None     Source Type: Journal    
DOI: 10.4103/0971-6866.32035     Document Type: Letter

References (4)

1. Radha Rama Devi A, Naushad SM, Prasad KC. Evaluation of total plasma homocysteine in Indian newborns using heel-prick samples. Indian J Pediatr 2006;73:503-8.
2. Kumar J, Das SK, Sharma P, Karthikeyan G, Ramakrishnan L, Sengupta S. Homocysteine levels are associated with MTHFR A1298C polymorphism in Indian population. J Hum Genet 2005;50:655-63.
3. Panigrahi I, Chatterjee T, Biswas A, Behari M, Choudhry PV, Saxena R. Role of MTHFR C677T polymorphism in ischemic stroke. Neurol India 2006;54:48-52.
4. Nair KG, Nair SR, Ashavaid TF, Dalal JJ, Eghlim FF. Methylenetetrahydrofolate reductase gene mutation and hyperhomocysteinemia as a risk factor for coronary heart disease in the Indian population. J Assoc Physicians India 2002;50:9-15.