DOI:
10.1055/s-00000077
Seminars in Thrombosis and Hemostasis
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References
Rosenberg N, Hauschner H, Peretz H , et al.
A 13-bp deletion in α(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia.
J Thromb Haemost 2005;
3 (12) 2764-2772
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