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Glanzmann thrombasthenia: genetic basis and clinical correlates
Glanzmann thrombasthenia (GT) is an autosomal recessive disorder of platelet aggregation caused by quantitative or qualitative defects in integrins αIIb and β3. These integrins are encoded by the ITGA2B and ITGB3 genes and form platelet glycoprotein (GP)IIb/IIIa, which acts as the principal platelet...
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| 出版年: | Haematologica |
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| 主要な著者: | , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Ferrata Storti Foundation
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7109743/ https://ncbi.nlm.nih.gov/pubmed/32139434 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3324/haematol.2018.214239 |
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