No Association between the Methyleletetrahydrofolate Reductase A1298C Variants and Atrial Fibrillation with Ischemic Stroke in Turkish Population

PP-138 The A1298C allele is characterized by a point mutation at position 1298 of the methyleletetrahydrofolate reductase (MTHFR) gene causing the replacement of glutamine by alanine in the corresponding enzyme. MTHFR gene A1298C mutation is associated with moderately elevated homocysteine levels.