Paroxysmal nocturnal hemoglobinuria due to hereditary nucleotide deletion in the HRF20 (CD59) gene
Version of Record online: 17 NOV 2005
Copyright © 1992 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
European Journal of Immunology
Volume 22, Issue 10, pages 2669–2673, October 1992
How to Cite
Motoyama, N., Okada, N., Yamashina, M. and Okada, H. (1992), Paroxysmal nocturnal hemoglobinuria due to hereditary nucleotide deletion in the HRF20 (CD59) gene. Eur. J. Immunol., 22: 2669–2673. doi: 10.1002/eji.1830221029
- Issue online: 17 NOV 2005
- Version of Record online: 17 NOV 2005
- Manuscript Revised: 8 JUL 1992
- Manuscript Received: 15 MAY 1992
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