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Characterization of aberrant splicing of von Willebrand factor in von Willebrand disease: an underrecognized mechanism
Approximately 10% of von Willebrand factor (VWF) gene mutations are thought to alter messenger RNA (mRNA) splicing through disruption of consensus splice sites. This mechanism is likely underrecognized and affected by mutations outside consensus splice sites. During VWF synthesis, splicing abnormali...
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| Publicado en: | Blood |
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| Autores principales: | , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
American Society of Hematology
2016
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4965908/ https://ncbi.nlm.nih.gov/pubmed/27317792 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2015-10-678052 |
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