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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 Yamashina¹, E Ueda, T Kinoshita, T Takami, A Ojima, H Ono, H Tanaka, N Kondo, T Orii, N Okada, et al.

Affiliations

PMID: 1699124
DOI: 10.1056/NEJM199010253231707

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. 1990.

Free article

. 1990 Oct 25;323(17):1184-9.

doi: 10.1056/NEJM199010253231707.

Authors

M Yamashina¹, E Ueda, T Kinoshita, T Takami, A Ojima, H Ono, H Tanaka, N Kondo, T Orii, N Okada, et al.

Affiliation

¹ Department of Pathology, Gifu University School of Medicine.

PMID: 1699124
DOI: 10.1056/NEJM199010253231707

No abstract available

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