Olsson P G, Rabbani H, Hammarström L, Smith C I
Centre for BioTechnology, NOVUM Karolinska Institute, Huddinge, Sweden.
Clin Exp Immunol. 1993 Oct;94(1):84-90. doi: 10.1111/j.1365-2249.1993.tb05982.x.
Fifteen patients with selective IgG1 deficiency were screened for immunoglobulin H chain C region locus (IGHC) gene deletions and three deletion haplotypes were found: del G1, del G1-G4 and del G4. These haplotypes, together with four deletion haplotypes described by us previously (del G1 (NY), del G1 (VIT) del G1-G2 (NY) and del G2-G4 (HJE)), were further characterized using pulsed-field gel electrophoresis (PFGE) to determine the physical extent of the deletions. The MluI fragment sizes confirmed the deletions, although the deduced sizes of the most extensive deletions indicated that material had been inserted into the locus.
对15例选择性IgG1缺乏患者进行免疫球蛋白重链C区基因座(IGHC)基因缺失筛查,发现了三种缺失单倍型:del G1、del G1-G4和del G4。这些单倍型与我们之前描述的四种缺失单倍型(del G1(NY)、del G1(VIT)、del G1-G2(NY)和del G2-G4(HJE))一起,使用脉冲场凝胶电泳(PFGE)进一步表征,以确定缺失的物理范围。MluI片段大小证实了缺失,尽管推断的最大缺失大小表明有物质插入到该基因座中。