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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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| Hlavní autoři: | , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
The National Academy of Sciences of the USA
1997
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC20027/ https://ncbi.nlm.nih.gov/pubmed/9050889 |
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