DOI:
10.1055/s-00035024
Thrombosis and Haemostasis
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References
Rosenberg N, Hauschner H, Peretz H. et al.
A 13-bp deletion in αIIb gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia.
J Thromb Haemost 2005;
03: 2764-2772.
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