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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Publicat a:Haematologica
Autors principals: 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
Idioma:Inglês
Publicat: Ferrata Storti Foundation 2020
Matèries:
Review Article
Accés en línia: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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