| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 2702326 | Journal of Stroke and Cerebrovascular Diseases | 2016 | 8 Pages |
Abstract
MTHFR c.677C>T is the predominant mutation and the only mutation that had patients with the homozygous mutant genotype. Venous thrombosis showed a significant association with the F5 c.1691G>A mutation.
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Authors
Hasini A. PhD, Dulika S. MBBS, MSc, Hemali W. MBBS, MD, Vajira H. MBBS, PhD,