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Response of Paroxysmal Nocturnal Hemoglobinuria Clone with Aplastic Anemia to Rituximab
Paroxysmal nocturnal hemoglobinuria is caused by expansion of a hematopoietic stem cell clone with an acquired somatic mutation in the PIG-A gene. This mutation aborts the synthesis and expression of the glycosylphosphatidylinositol anchor proteins CD55 and CD59 on the surface of blood cells, thereb...
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| Autori principali: | , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Hindawi Publishing Corporation
2012
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| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3420688/ https://ncbi.nlm.nih.gov/pubmed/22937317 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/106182 |
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