Hemoglobin Pyrgos (β83 GLY→ASP) in a Japanese Family
作者:
YamadaH.,
HottaT.,
OhbaY.,
MiyajiT.,
ItoJ.,
MinamiH.,
期刊:
Hemoglobin
(Taylor Available online 1977)
卷期:
Volume 1,
issue 3
页码: 245-255
ISSN:0363-0269
年代: 1977
DOI:10.3109/03630267709003407
出版商: Taylor&Francis
数据来源: Taylor
摘要:
A screening survey for abnormal hemoglobins at a hospital in Mizunami city, Gifu prefecture, Japan detected a fast-moving variant of hemoglobin in a family of Japanese origin. The abnormal hemoglobin constitutes about 45 percent of the total hemoglobin from the propositus and another carrier in the family, but neither of these persons had anemia, jaundice, cyanosis or splenomegaly. Structural analysis of this hemoglobin revealed that the amino acid substitution vas at residue 83 in theβchain, where a glycine was replaced by an aspartic acid. Thin hemoglobin variant has been previously reported in a Greek child (hemoglobin Pyrgos) (1). Oxygen affinity of hemoglobin Pyrgos was found to be normal.
点击下载:
PDF (274KB)
返 回