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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Detalles Bibliográficos
Autores principales: Raghupathy, Radha, Derman, Olga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420688/
https://www.ncbi.nlm.nih.gov/pubmed/22937317
http://dx.doi.org/10.1155/2012/106182

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420688/
https://www.ncbi.nlm.nih.gov/pubmed/22937317
http://dx.doi.org/10.1155/2012/106182

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