These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. [Analysis of the GPIIb and GPIIIa genes in patients with Glanzmann's thrombasthenia]. Yasunaga M, Ryo R, Adachi M, Sugano W, Yoshida A, Nakayama K, Saigo K, Yasunaga K, Yamaguchi N. Rinsho Ketsueki; 1992 Feb; 33(2):133-8. PubMed ID: 1635160 [Abstract] [Full Text] [Related]
8. Biochemical and molecular basis of Glanzmann's thrombasthenia. Perutelli P, Mori PG. Haematologica; 1992 Jan; 77(5):421-6. PubMed ID: 1483593 [Abstract] [Full Text] [Related]
9. Identification of an abnormal gene for the GPIIIa subunit of the platelet fibrinogen receptor resulting in Glanzmann's thrombasthenia. Bray PF, Shuman MA. Blood; 1990 Feb 15; 75(4):881-8. PubMed ID: 1967954 [Abstract] [Full Text] [Related]
10. Homozygous Cys542-->Arg substitution in GPIIIa in a Swiss patient with type I Glanzmann's thrombasthenia. Ruan J, Schmugge M, Clemetson KJ, Cazes E, Combrie R, Bourre F, Nurden AT. Br J Haematol; 1999 May 15; 105(2):523-31. PubMed ID: 10233432 [Abstract] [Full Text] [Related]
11. A Cys374Tyr homozygous mutation of platelet glycoprotein IIIa (beta 3) in a Chinese patient with Glanzmann's thrombasthenia. Grimaldi CM, Chen F, Scudder LE, Coller BS, French DL. Blood; 1996 Sep 01; 88(5):1666-75. PubMed ID: 8781422 [Abstract] [Full Text] [Related]
12. Application of GPIIIa gene Taq I polymorphism to determination of carrier status in Glanzmann's thrombasthenia families of Chinese origin. Ruan C, Gu J, Wang X, Chu X, Pan J. Thromb Haemost; 1993 Jan 11; 69(1):64-9. PubMed ID: 8095357 [Abstract] [Full Text] [Related]
14. An exon 28 mutation resulting in alternative splicing of the glycoprotein IIb transcript and Glanzmann's thrombasthenia. Iwamoto S, Nishiumi E, Kajii E, Ikemoto S. Blood; 1994 Feb 15; 83(4):1017-23. PubMed ID: 8111043 [Abstract] [Full Text] [Related]