Hemoglobin Bethesda Causing Polycythemia in a Japanese Family.
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概要
- 論文の詳細を見る
A family with Hemoglobin Bethesda is reported. A 23-year-old man was hospitalized for the evaluation of polycythemia. Analysis of hemoglobin using high pressure liquid chromatography showed the presence of hemoglobinopathy. Separation of globin into α and β chains revealed approximately 50% of the β chain to be abnormal. Analysis of the DNA sequence of the β chain gene identified Hb Bethesda. The family study disclosed that his father and sister also had the same hemoglobinopathy. This case is the first report of Hb Bethesda in Japan.(Internal Medicine 33: 242-247, 1994)
- 社団法人 日本内科学会の論文
著者
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Matsuoka Yasuo
The Department Of Internal Medicine
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Harano Teruo
The Department Of Biochemistry Kawasaki Medical College
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HANADA Tetsuya
the Department of Internal Medicine, Kawasaki Municipal Hospital
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IRIMAJIRI Shoichiro
the Department of Internal Medicine, Kawasaki Municipal Hospital
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KAWASHIMA Issei
The Department of Internal Medicine, Kawasaki Municipal Hospital
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ARIMA Koichiro
the Department of Internal Medicine, Kawasaki Municipal Hospital
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HARADA Keiichi
the Department of Internal Medicine, Kawasaki Municipal Hospital
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