Hassan H J, Leonardi A, Guerriero R, Chelucci C, Cianetti L, Ciavarella N, Ranieri P, Pilolli D, Peschle C
Blood. 1985 Sep;66(3):728-30.
The structure of factor IX gene was analyzed in a hemophilia B patient with inhibitor. Genomic DNA, digested with a variety of restriction endonucleases, was hybridized with the cDNA and various genomic factor IX probes. A large subtotal deletion of the gene was observed. The borders of the deletion span from a approximately 125 nucleotide region within the last exon to an unknown domain at least 7.5 kb upstream from the first exon: it thus involves approximately 33 kb of the factor IX locus. The abnormal gene was inherited by the daughter of the propositus, who showed both the normal and the deleted allele.
对一名患有抑制物的B型血友病患者的凝血因子IX基因结构进行了分析。用多种限制性内切酶消化基因组DNA,使其与cDNA及各种基因组凝血因子IX探针杂交。观察到该基因存在大片段的部分缺失。缺失的边界范围从最后一个外显子内大约125个核苷酸区域到第一个外显子上游至少7.5 kb的一个未知区域:因此它涉及凝血因子IX基因座约33 kb的区域。先证者的女儿遗传了这个异常基因,她同时显示出正常和缺失的等位基因。