Tongio M M, Mayer S, Hauptmann G, North M L, Koehl C, Abecassis J, Mandel P, Wertenschlag J
Tissue Antigens. 1979 Apr;13(4):273-7. doi: 10.1111/j.1399-0039.1979.tb00795.x.
Forty-six members of a family known to have Porphyria were studied. As the disease is often latent clinically, erythrocyte uroporphyrinogen I synthetase activity was determined to classify the subjects as being healthy or carriers. HLA--A, B, C, Bf, GLO antigens were determined. No linkage between acute intermittent Porphyria and the HLA system was noted in this family.
对一个已知患有卟啉症的家族中的46名成员进行了研究。由于该疾病在临床上常常呈潜伏状态，因此测定了红细胞尿卟啉原I合成酶的活性，以便将这些受试者分类为健康者或携带者。测定了HLA - A、B、C、Bf、GLO抗原。在这个家族中未发现急性间歇性卟啉症与HLA系统之间存在连锁关系。
