Glanzmann thrombasthenia: the need for epidemiological studies
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2009.03597.x/fullpdf
Reference17 articles.
1. Identification of an abnormal gene for the GPIIIa subunit of the platelet fibrinogen receptor resulting in Glanzmann thrombasthenia;Bray;Blood,1990
2. The molecular genetic basis of Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel;Newman;Proc Natl Acad Sci USA,1991
3. Two novel mutations in the alphaIIb calcium-binding domains identify hydrophobic regions essential for alphaIIbbeta3 biogenesis;Mitchell;Blood,2003
4. A 13-bp deletion in alphaIIb gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia;Rosenberg;J Thromb Haemost,2005
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