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A Case Report on an Extremely Rare Disease: Factor XI Deficiency
Factor XI deficiency is a rare condition with an estimated prevalence of about one in one million and is more commonly seen in Ashkenazi Jews (8-9%) due to consanguinity. It occurs because of mutations in the factor XI gene (F11) on chromosome 4(4q35). Patients with this disorder may remain asymptom...
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| Vydáno v: | Cureus |
|---|---|
| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Cureus
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7603878/ https://ncbi.nlm.nih.gov/pubmed/33150098 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7759/cureus.10746 |
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