(Q28264911)

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Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria

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Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria (English)
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M Yamashina
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E Ueda
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T Kinoshita
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T Takami
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A Ojima
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H Ono
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H Tanaka
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N Kondo
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T Orii
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N Okada
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25 October 1990
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323
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17
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1184-9
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