Genetic defects underlying paroxysmal nocturnal hemoglobinuria that arises out of aplastic anemia. [electronic resource]
Producer: 19960213Description: 4656-61 p. digitalISSN:- 0006-4971
- Anemia, Aplastic -- complications
- Antilymphocyte Serum -- therapeutic use
- Base Sequence
- Cyclosporine -- therapeutic use
- DNA Mutational Analysis
- Hemoglobinuria, Paroxysmal -- etiology
- Humans
- Immunosuppressive Agents -- therapeutic use
- Membrane Proteins -- deficiency
- Molecular Sequence Data
- Point Mutation
- Polymerase Chain Reaction
- RNA Splicing
- RNA, Messenger -- genetics
- Sequence Deletion
- T-Lymphocytes
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Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
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