Methylenetetrahydrofolate reductase homozygous mutation in a young boy with cerebellar infarction
Posterior circulation vascular occlusive disease in children is a rare and uncommonly reported event. Among the numerous risk factors, the methylenetetrahydrofolate reductase (MTHFR) mutation is considered to be a common genetic cause of thrombosis in adults and children. Recently, a link between th...
| Main Authors: | , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2009-11-01
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| Series: | Pediatric Reports |
| Online Access: | http://www.pagepress.org/journals/index.php/pr/article/view/785 |