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Spontaneously developed paraplegia in a patient with Factor V Leiden mutation
Factor V Leiden (FVL) mutation is the one-point mutation in G1691A in the tenth exon of the gene for Factor V, caused by the substitution of glutamine for arginine at codon 506. We present here a patient with a mutation of the Factor V gene and taking anticoagulant therapy, who became paraplegic fol...
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| Vydáno v: | Spinal Cord Ser Cases |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Nature Publishing Group
2016
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5129424/ https://ncbi.nlm.nih.gov/pubmed/28053741 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/scsandc.2015.39 |
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