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Abnormal expression and mutation of the RBPJ gene may be involved in CD59(−) clonal proliferation in paroxysmal nocturnal hemoglobinuria
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal proliferative disease of hematopoietic stem cells. Various gene mutations, including the phosphatidylinositol glycan anchor biosynthesis class A (PIG-A) gene, may contribute to the proliferation of PNH clones. In order to explore the me...
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| Publicado en: | Exp Ther Med |
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| Autores principales: | , , , , , , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
D.A. Spandidos
2019
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6489004/ https://ncbi.nlm.nih.gov/pubmed/31086586 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2019.7475 |
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