Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria (Q28264911)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria |
scientific article |
Statements
Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria (English)
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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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