Mutations of von Willebrand factor gene in families with von Willebrand disease in the Aland Islands.
Patients with von Willebrand disease in four families in the Aland Islands, including the original family that was described in 1926 by the Finnish physician von Willebrand, were screened for mutations in the Swedish "hot-spot" regions (exons 18, 28, 32, 43, and 45) of the von Willebrand factor gene...
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| Publicat a: | Proc Natl Acad Sci U S A |
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| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
National Academy of Sciences
1993
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC47262/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8367445/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.90.17.7937 |
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