Molecular basis of human von Willebrand disease: analysis of platelet von Willebrand factor mRNA.
von Willebrand disease (vWD), the most common inherited bleeding disorder in humans, can result from either a quantitative or a qualitative defect in the adhesive glycoprotein, von Willebrand factor (vWF). Molecular studies of vWD have been limited by the large size of the vWF gene and difficulty in...
保存先:
| 出版年: | Proc Natl Acad Sci U S A |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
National Academy of Sciences
1989
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC287212/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2786201/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.86.10.3723 |
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