Yang S Y, Coleman P, Ochs H D, Dupont B
Hum Genet. 1981;57(3):307-11. doi: 10.1007/BF00278950.
The genetic polymorphism of the vitamin B12 transport protein transcobalamin II (TC II) was studied in the Caucasian population and in families. There are five codominent alleles of TC II which show a Mendelian mode of inheritance. No genetic linkage of TC II was found with gene loci for ADA, GLO I, Pi, HLA, AB0 and AK1. TC II like proteins could be detected on autoradiograph of PAGE in two patients with congenital homozygosity for functional TC II deficiency. These vitamin B12 binding proteins in the patients' serum were shown not to be normal R-proteins.
在高加索人群及家族中研究了维生素B12转运蛋白转钴胺素II(TC II)的遗传多态性。TC II有五个共显性等位基因,呈孟德尔遗传模式。未发现TC II与ADA、GLO I、Pi、HLA、AB0和AK1的基因座存在遗传连锁关系。在两名功能性TC II缺乏的先天性纯合子患者的PAGE放射自显影片上可检测到类似TC II的蛋白质。患者血清中的这些维生素B12结合蛋白显示并非正常的R蛋白。