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Rapid discrimination of the phenotypic variants of von Willebrand disease
Approximately 20% to 25% of patients with von Willebrand disease (VWD) have a qualitative defect of the von Willebrand factor (VWF) protein activities. Variant VWD typically is classified as type 1C, 2A, 2B, 2M, or 2N depending on the VWF activity defect. Traditionally, diagnosis has relied on multi...
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| 出版年: | Blood |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Society of Hematology
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4874227/ https://ncbi.nlm.nih.gov/pubmed/26917779 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2015-11-664680 |
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