Complement in paroxysmal nocturnal hemoglobinuria: exploiting our current knowledge to improve the treatment landscape
Author:
Publisher
Informa UK Limited
Subject
Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1586/17474086.2014.953926
Reference88 articles.
1. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria
2. The Cloning of PIG-A, a Component in the Early Step of GPI-Anchor Biosynthesis
3. Somatic Mutations in Paroxysmal Nocturnal Hemoglobinuria: A Blessing in Disguise?
4. A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGT
5. Abnormal T-cell repertoire is consistent with immune process underlying the pathogenesis of paroxysmal nocturnal hemoglobinuria
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