Identification of three novel pathogenic ITGA2B and one novel pathogenic ITGB3 mutations in patients with hereditary Glanzmann’s thrombasthenia living in Eastern Turkey

Glanzmann’s thrombasthenia (GT) is an autosomal recessive disorder in which the underlying problem is the lack or dysfunction of the GpIIb/IIIa receptor on the platelet surface. The present study determines the genetic mutation typology and analyzes the association between mutation types and clinica...

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Bibliografische Detailangaben

Hauptverfasser:	Kamuran Karaman, Eyüp Yürektürk, Hadi Geylan, Akkız Şahin Yaşar, Serap Karaman, Huri Sema Aymelek, Mecnun Çetin, Ahmet Fayik Oner
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	Taylor & Francis Group 2021-02-01
Schriftenreihe:	Platelets
Schlagworte:	glanzmann thrombasthenia gpiib/iiia novel mutation tgb3
Online-Zugang:	http://dx.doi.org/10.1080/09537104.2020.1732331
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