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Modifiers of von Willebrand factor identified by natural variation in inbred strains of mice
Type 1 von Willebrand disease (VWD) is the most common inherited human bleeding disorder. However, diagnosis is complicated by incomplete penetrance and variable expressivity, as well as wide variation in von Willebrand factor (VWF) levels among the normal population. Previous work has exploited the...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
American Society of Hematology
2009
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2796139/ https://ncbi.nlm.nih.gov/pubmed/19789385 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2009-07-233213 |
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