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.
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| Description | scientific article published in May 2005 |
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author: Istvan Balogh |
| Publication date | May 1, 2005 |
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