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Glanzmann thrombasthenia

Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding syndrome affecting the megakaryocyte lineage and characterized by lack of platelet aggregation. The molecular basis is linked to quantitative and/or qualitative abnormalities of αIIbβ3 integrin. This receptor mediates the binding o...

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Bibliografske podrobnosti
Glavni avtor: Nurden, Alan T
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2006
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1475837/
https://ncbi.nlm.nih.gov/pubmed/16722529
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-1-10
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