Characterization of the cDNA Encoding alphaIIb and beta3 in normal horses and two horses with Glanzmann thrombasthenia

Vet Pathol. 2006 Jan;43(1):78-82. doi: 10.1354/vp.43-1-78.

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.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Base Sequence
  • DNA Primers
  • DNA, Complementary / genetics*
  • Horse Diseases / genetics*
  • Horses
  • Integrin beta3 / genetics*
  • Molecular Sequence Data
  • Platelet Membrane Glycoprotein IIb / genetics*
  • Sequence Analysis, DNA / veterinary
  • Thrombasthenia / genetics
  • Thrombasthenia / veterinary*

Substances

  • DNA Primers
  • DNA, Complementary
  • Integrin beta3
  • Platelet Membrane Glycoprotein IIb