Novel and recurrent mutations of ITGA2B and ITGB3 genes in Korean patients with Glanzmann thrombasthenia

Pediatric Blood & Cancer, 05/04/2012

Glanzmann thrombasthenia (GT) is an autosomal recessive bleeding disorder caused by defective glycoprotein, alphaIIb and beta3, encoded by ITGA2B and ITGB3 genes, respectively.

Print Article Summary Cat 2 CME Report