Clinical and molecular insights into Glanzmann's thrombasthenia in China

Author:

Zhou L.123ORCID,Jiang M.13,Shen H.13,You T.13,Ding Z.13,Cui Q.13,Ma Z.13,Yang F.13,Xie Z.13,Shi H.13,Su J.13,Cao L.13,Lin J.13,Yin J.13,Dai L.13,Wang H.4,Wang Z.13,Yu Z.13,Ruan C.13,Xia L.135

Affiliation:

1. Key Laboratory of Thrombosis & Hemostasis of Ministry of Health, Jiangsu Institute of Hematology; The First Affiliated Hospital of Soochow University; Suzhou China

2. Hematology department, Affiliated Hospital of Nantong University; Nantong China

3. Collaborative Innovation Center of Hematology; Soochow University; Suzhou China

4. Department of Pediatrics/Section of Genetics; University of Oklahoma Health Sciences Center; Oklahoma City Oklahoma

5. Cardiovascular Biology Research Program; Oklahoma Medical Research Foundation; Oklahoma City Oklahoma

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference33 articles.

1. Glanzmann's thrombasthenia (defective platelet integrin alphaIIb-beta3): proposals for management between evidence and open issues;Di Minno;Thromb Haemost,2009

2. Glanzmann's thrombasthenia: the spectrum of clinical disease;George;Blood,1990

3. Glanzmann thrombasthenia;Nurden;Orphanet J Rare Dis,2006

4. Different biochemical expression pattern of platelet surface glycoproteins suggests molecular diversity of Glanzmann's thrombasthenia in Iran;Farsinejad;Blood Coagul Fibrinolysis,2013

5. Glanzmann's thrombasthenia: modulation of clinical phenotype by alpha2C807T gene polymorphism;D'Andrea;Haematologica,2003

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