Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann’s thrombasthenia
Author:
Publisher
Informa UK Limited
Subject
Hematology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/09537104.2014.998994
Reference11 articles.
1. Glanzmann’s thrombasthenia (defective platelet integrin αIIb-β3): proposals for management between evidence and open issues
2. Molecular basis of Glanzmann's Thrombasthenia and current strategies in treatment
3. Glanzmann's Thrombasthenia: An Overview
4. Hematologically Important Mutations: Glanzmann Thrombasthenia
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2. Glanzmann Thrombasthenia: Diagnosis and Management;Congenital Bleeding Disorders;2023
3. Flow cytometric analysis of platelet surface glycoproteins in the diagnosis of thirty-two Turkish patients with Glanzmann thrombasthenia: a multicenter experience;TURKISH JOURNAL OF MEDICAL SCIENCES;2021-08-30
4. Identification of three novel pathogenic ITGA2B and one novel pathogenic ITGB3 mutations in patients with hereditary Glanzmann’s thrombasthenia living in Eastern Turkey;Platelets;2020-02-22
5. Identification of one novel pathogenic ITGB3 mutation and two known mutations in two Chinese pedigrees with hereditary Glanzmann thrombasthenia;Platelets;2019-05-14
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