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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Bibliografski detalji
Izdano u:Haematologica
Glavni autori: Botero, Juliana Perez, Lee, Kristy, Branchford, Brian R, Bray, Paul F, Freson, Kathleen, Lambert, Michele P., Luo, Minjie, Mohan, Shruthi, Ross, Justyne E., Bergmeier, Wolfgang, Di Paola, Jorge
Format: Artigo
Jezik:Inglês
Izdano: Ferrata Storti Foundation 2020
Teme:
Review Article
Online pristup: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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