Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria.
作者信息
Yamashina M, Ueda E, Kinoshita T, Takami T, Ojima A, Ono H, Tanaka H, Kondo N, Orii T, Okada N
机构信息
Department of Pathology, Gifu University School of Medicine.
出版信息
N Engl J Med. 1990 Oct 25;323(17):1184-9. doi: 10.1056/NEJM199010253231707.
PMID:1699124
Abstract
摘要
Zotero 插件