Inherited complete deficiency of 20-kilodalton homologous restriction factor (CD59) as a cause of paroxysmal nocturnal hemoglobinuria. [electronic resource]
Producer: 19901121Description: 1184-9 p. digitalISSN:- 0028-4793
- Acetylcholinesterase -- analysis
- Adult
- Blood Proteins -- analysis
- CD55 Antigens
- CD59 Antigens
- Carrier Proteins -- analysis
- Cell Separation
- Cells, Cultured
- Erythrocyte Membrane -- chemistry
- Fibroblasts -- chemistry
- Flow Cytometry
- Hemoglobinuria, Paroxysmal -- blood
- Humans
- Immunohistochemistry
- Male
- Membrane Proteins -- analysis
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Publication Type: Case Reports; Journal Article
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