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...
Spremljeno u:
| Izdano u: | Proc Natl Acad Sci U S A |
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| Glavni autori: | , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
National Academy of Sciences
1989
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| Teme: | |
| Online pristup: | 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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