A genetic analysis of integrin function: Glanzmann thrombasthenia in vitro
Glanzmann thrombasthenia, an inherited bleeding disorder, can be caused by a defect or deficiency in platelet integrin α(IIb)β(3) (GPIIb-IIIa). Studies of thrombasthenia variants have facilitated identification of sites involved in the functions of α(IIb)β(3) and other integrins. Such sites include...
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| Veröffentlicht in: | Proc Natl Acad Sci U S A |
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| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
National Academy of Sciences
1997
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| Schlagworte: | |
| Online-Zugang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC20027/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9050889/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.94.5.1973 |
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