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Hemoglobin
international journal for hemoglobin research
Volume 12, 1988 - Issue 5-6
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Original Article

A β+-Thalassemia (Codon 24, GGT → GGA) Found in a Japanese

Y. Hattori Department of Clinical Laboratory Sciences, Yamaguchi University School of Medicine 1144 Kogushi, Ube Yamaguchi, 755, Japan
,
Y. Yamashiro Department of Clinical Laboratory Sciences, Yamaguchi University School of Medicine 1144 Kogushi, Ube Yamaguchi, 755, Japan
,
Y. Matsuno Department of Clinical Laboratory Sciences, Yamaguchi University School of Medicine 1144 Kogushi, Ube Yamaguchi, 755, Japan
,
Y. Ohba Department of Clinical Laboratory Sciences, Yamaguchi University School of Medicine 1144 Kogushi, Ube Yamaguchi, 755, Japan
,
T. Miyaji Department of Clinical Laboratory Sciences, Yamaguchi University School of Medicine 1144 Kogushi, Ube Yamaguchi, 755, Japan
,
Ki. Yamamoto Yamaguchi University School of A11ied Health Sciences, Ube, Yamaguchi, Japan
,
Ku. Yamamoto Yamaguchi University School of A11ied Health Sciences, Ube, Yamaguchi, Japan
,
M. Omine Third Department of Internal Medicine, Gunma University School of Medicine, Maebashi, Gunma, Japan
&
I. Shimda Asama Hospital, Saku, Nagano, Japan
 show all
Pages 655-660 | Received 11 Nov 1987, Accepted 01 Jun 1988, Published online: 07 Jul 2009
 
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Abstract

A β+-thalassemia mutation at codon 24 (GGT→GGA) was discovered in a Japanese; this is the third type of β-thalassemia found in this population. The case, as well as the data from DNA sequencing analysis, are presented.

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