Fuyuno K, Torigoe T, Ohba Y, Matsuoka M, Miyaji T
Hemoglobin. 1981;5(2):139-51. doi: 10.3109/03630268108996920.
Two gamma chain variants were discovered during a survey of 2,569 cord bloods of Japanese. One was the first case with mutation of the T-gamma chain, i. e. Hb F Yamaguchi or gamma 80 (EF 4) Asp leads to Asn (75 Thr, 136 Ala). It comprised 33.6% of Hb F, an unusually high percentage for a gamma chain variant. The other concerned with the first report of substitution at E 16, i. e. Hb F Iwata or gamma 72 (E 16) Gly leads to Arg (75 Ile, 136 Ala). It comprised 11.0% which is comparable to the values usually reported in an A-gamma chain variant. No clinical consequences have been observed in association with the hemoglobin variants.
在对2569份日本脐带血的调查中发现了两种γ链变体。一种是首例T-γ链发生突变的情况,即Hb F山口型或γ80(EF 4)天冬氨酸突变为天冬酰胺(75位苏氨酸,136位丙氨酸)。它占Hb F的33.6%,对于γ链变体来说,这一比例异常高。另一种是首次报道的E 16位发生替换的情况,即Hb F岩田型或γ72(E 16)甘氨酸突变为精氨酸(75位异亮氨酸,136位丙氨酸)。它占11.0%,这一数值与通常报道的A-γ链变体的值相当。尚未观察到与这些血红蛋白变体相关的临床后果。