A 13-bp deletion in αIIb gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia

N. Rosenberg, H. Hauschner, H. Peretz, R. Mor-Cohen, M. Landau, B. Shenkman, G. Kenet, B. S. Coller, A. A. Awidi, U. Seligsohn

Research output: Contribution to journal › Article › peer-review

41 Scopus citations

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Biochemistry, Genetics and Molecular Biology