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» New ITGA2B gene compound heterozygous mutation found in Glanzmann thrombasthenia
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Biomarkers
New ITGA2B gene compound heterozygous mutation found in Glanzmann thrombasthenia
Feb. 10, 2023
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Glanzmann thrombasthenia (GT) is a rare bleeding disorder caused by defects in the expression of platelet surface integrins, such as integrin alpha-IIb (GPIIb, encoded by
ITGA2B
).
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