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Case Reports
. 1990 Oct 25;323(17):1184-9.
doi: 10.1056/NEJM199010253231707.

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

M Yamashina  1 , E Ueda, T Kinoshita, T Takami, A Ojima, H Ono, H Tanaka, N Kondo, T Orii, N Okada, et al.
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Free article
Case Reports

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

M Yamashina et al. N Engl J Med. .
Free article
No abstract available

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