Nagarajan, S <br/><br/>
Genetic defects underlying paroxysmal nocturnal hemoglobinuria that arises out of aplastic anemia.  [electronic resource] 

 -  Blood  Dec 1995 
 - 4656-61 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anemia, Aplastic--complications<br/>Antilymphocyte Serum--therapeutic use<br/>Base Sequence<br/>Cyclosporine--therapeutic use<br/>DNA Mutational Analysis<br/>Hemoglobinuria, Paroxysmal--etiology<br/>Humans<br/>Immunosuppressive Agents--therapeutic use<br/>Membrane Proteins--deficiency<br/>Molecular Sequence Data<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>RNA Splicing<br/>RNA, Messenger--genetics<br/>Sequence Deletion<br/>T-Lymphocytes