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Q38183490-1FC1C156-DDF2-4C29-9882-CFA9B22708E0
Q38183490-1FC1C156-DDF2-4C29-9882-CFA9B22708E0
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http://www.wikidata.org/entity/statement/Q38183490-1FC1C156-DDF2-4C29-9882-CFA9B22708E0
What is the role of genetic testing in the investigation of patients with suspected platelet function disorders?
P2860
Q38183490-1FC1C156-DDF2-4C29-9882-CFA9B22708E0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38183490-1FC1C156-DDF2-4C29-9882-CFA9B22708E0
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wasDerivedFrom
5f95a3b4a1eb5474fefaa264bd742e0aba6abe7b
P2860
A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia.