Inherited Complete Deficiency of 20-Kilodalton Homologous Restriction Factor (CD59) as a Cause of Paroxysmal Nocturnal Hemoglobinuria-Reference-Cited by-同舟云学术

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Inherited Complete Deficiency of 20-Kilodalton Homologous Restriction Factor (CD59) as a Cause of Paroxysmal Nocturnal Hemoglobinuria

Published:1990-10-25 Issue:17 Volume:323 Page:1184-1189
ISSN:0028-4793
Container-title:New England Journal of Medicine
language:en
Short-container-title:N Engl J Med

Author:

Yamashina Manabu,Ueda Etsuko,Kinoshita Taroh,Takami Tsuyoshi,Ojima Akitsugu,Ono Hiromasa,Tanaka Hiroshi,Kondo Naomi,Orii Tadao,Okada Noriko,Okada Hidechika,Inoue Kozo,Kitani Teruo

Publisher

Massachusetts Medical Society

Subject

General Medicine

Link

http://www.nejm.org/doi/pdf/10.1056/NEJM199010253231707

Cited by 315 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

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2. Paroxysmal Nocturnal Hemoglobinuria, Pathophysiology, Diagnostics, and Treatment;TRANSFUS MED HEMOTH;2024

3. Integrated Applied Clinical Pharmacology in the Advancement of Rare and Ultra‐Rare Disease Therapeutics;Clinical Pharmacology & Therapeutics;2024-07-22

4. CD59 gene: 143 haplotypes of 22,718 nucleotides length by computational phasing in 113 individuals from different ethnicities;Transfusion;2024-05-30

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