Yamashina, M <br/><br/>
Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria.  [electronic resource] 

 -  The New England journal of medicine  Oct 1990 
 - 1184-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0028-4793 
<br/><br/><label>Standard No.: </label>10.1056/NEJM199010253231707  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acetylcholinesterase--analysis<br/>Adult<br/>Blood Proteins--analysis<br/>CD55 Antigens<br/>CD59 Antigens<br/>Carrier Proteins--analysis<br/>Cell Separation<br/>Cells, Cultured<br/>Erythrocyte Membrane--chemistry<br/>Fibroblasts--chemistry<br/>Flow Cytometry<br/>Hemoglobinuria, Paroxysmal--blood<br/>Humans<br/>Immunohistochemistry<br/>Male<br/>Membrane Proteins--analysis