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

Ítems similars

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