Naparstek Y, Abrahamov A, Cohen T, Brautbar C
Am J Hematol. 1984 Aug;17(2):113-6. doi: 10.1002/ajh.2830170203.
Three generations of a Jewish family with hereditary thrombocytopenia (HT) are described. The disease was manifested clinically by mild bleeding tendency since infancy. Circumcision, however, did not result in excessive bleeding. HLA study in this family indicated that the HT locus is not linked to HLA.
本文描述了一个患有遗传性血小板减少症(HT)的犹太家族的三代人。自婴儿期起,该疾病在临床上表现为轻度出血倾向。然而,包皮环切术并未导致过度出血。对这个家族的HLA研究表明,HT基因座与HLA不连锁。