Hematologically important mutations: Glanzmann thrombasthenia

被引:74
作者
French, DL [1 ]
Coller, BS [1 ]
机构
[1] CUNY MT SINAI SCH MED,DEPT MED,NEW YORK,NY 10029
关键词
D O I
10.1006/bcmd.1997.0117
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:39 / 51
页数:13
相关论文
共 65 条
  • [1] [Anonymous], 1997, COMMUNICATION
  • [2] BAJT ML, 1992, J BIOL CHEM, V267, P3789
  • [3] Basani R. B., 1996, Blood, V88, p32A
  • [4] Basani RB, 1996, BLOOD, V88, P167
  • [5] Beaudet AL, 1996, HUM MUTAT, V8, P197
  • [6] Beutler E, 1996, HUM MUTAT, V8, P203, DOI 10.1002/(SICI)1098-1004(1996)8:3<203::AID-HUMU1>3.3.CO
  • [7] 2-C
  • [8] BOURRE R, 1995, BLOOD, V86, pA452
  • [9] BRAY PF, 1990, BLOOD, V75, P881
  • [10] A DELETION IN THE GENE FOR GLYCOPROTEIN-IIB ASSOCIATED WITH GLANZMANN THROMBASTHENIA
    BURK, CD
    NEWMAN, PJ
    LYMAN, S
    GILL, J
    COLLER, BS
    PONCZ, M
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (01) : 270 - 276