A deletion in the gene for glycoprotein IIb associated with Glanzmann's thrombasthenia.

Gelijkaardige items

• Glanzmann thrombasthenia secondary to a Gly273-->Asp mutation adjacent to the first calcium-binding domain of platelet glycoprotein IIb.
  door: Poncz, M, et al.
  Gepubliceerd in: (1994)
• The molecular genetic basis of Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel.
  door: Newman, P J, et al.
  Gepubliceerd in: (1991)
• A variant of Glanzmann's thrombasthenia with abnormal glycoprotein IIb-IIIa complexes in the platelet membrane.
  door: Nurden, A T, et al.
  Gepubliceerd in: (1987)
• A 13-bp deletion in α(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia
  door: ROSENBERG, N., et al.
  Gepubliceerd in: (2005)
• Monocytes and platelets share the glycoproteins IIb and IIIa that are absent from both cells in Glanzmann's thrombasthenia type I.
  door: Gogstad, G, et al.
  Gepubliceerd in: (1983)