Flow cytometric analysis of platelet surface glycoproteins in the diagnosis of thirty-two Turkish patients with Glanzmann thrombasthenia: a multicenter experience

BACKGROUND/AIM: Glanzmann thrombasthenia (GT) is a rare autosomal recessively inherited bleeding disorder characterized by the quantitative (type 1 and type 2) or qualitative (type 3) deficiency in platelet membrane glycoprotein (GP) IIb/IIIa (CD41a/CD61) fibrinogen receptors. In type 1, 2, and 3, C...

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Detalles Bibliográficos
Autores principales: SARAYMEN, Berkay, MUHTAROĞLU, Sabahattin, KÖKER, Mustafa Yavuz, SARPER, Nazan, ZENGİN, Emine, ALBAYRAK, Canan, ALBAYRAK, Davut, ZÜLFİKAR, Bülent, KOÇ ŞENOL, Başak, BENTLİ, Esma, YILMAZ, Semih, ÇETİN, Aysun, ESER, Bülent, ÇETİN, Mustafa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8569771/
https://www.ncbi.nlm.nih.gov/pubmed/33957723
http://dx.doi.org/10.3906/sag-2006-107

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8569771/
https://www.ncbi.nlm.nih.gov/pubmed/33957723
http://dx.doi.org/10.3906/sag-2006-107

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