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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...
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| Hoofdauteurs: | , , , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
PAGEPress Publications
2009
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3096031/ https://ncbi.nlm.nih.gov/pubmed/21589820 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4081/pr.2009.e4 |
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