Abstract
Glanzmann thrombasthenia (GT) is an inherited, intrinsic platelet defect characterized by a quantitative or qualitative change in the platelet glycoprotein complex IIb-IIIa (integrin alpha(IIb)beta3). The subunits are encoded by separate genes and both subunits must be expressed for a stable complex to form on the platelet surface; therefore, a defect in either gene can result in GT.
MeSH terms
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Animals
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Base Sequence
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DNA Primers
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DNA, Complementary / genetics*
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Horse Diseases / genetics*
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Horses
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Integrin beta3 / genetics*
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Molecular Sequence Data
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Platelet Membrane Glycoprotein IIb / genetics*
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Sequence Analysis, DNA / veterinary
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Thrombasthenia / genetics
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Thrombasthenia / veterinary*
Substances
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DNA Primers
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DNA, Complementary
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Integrin beta3
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Platelet Membrane Glycoprotein IIb