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A novel homozygous mutation (1619delC) in GPIIb gene associated with Glanzmann thrombasthenia, the decay of GPIIb-mRNA and the synthesis of a truncated GPIIb unable to form complex with GPIIIa.
scientific article published in May 2005
Author/s
author: Istvan Balogh, János Kappelmayer
Work details
Publication date
May 1, 2005
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