A family of hereditary xanthinuria: Two siblings with peptic ulcer and hypouricemia due to xanthine oxidase deficinecy, and a heterozygote(father) with gout.
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概要
著者
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河野 典夫
大阪大学医学部保健学科
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垂井 清一郎
大阪大学医学部小児科学教室
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宮崎 都志幸
済生会中津病院内科
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姫野 誠一
大阪大学医学部第二内科
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原 尚子
大阪大学医学部第二内科
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嶺尾 郁夫
大阪大学医学部第二内科
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清川 裕朗
大阪大学医学部第二内科
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川知 雅典
大阪大学医学部第二内科
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山田 祐也
大阪大学医学部第二内科
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垂井 清一郎
大阪大学医学部中央臨床検査部
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姫野 誠一
大阪大学医学部第2内科
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