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Bone marrow fibrosis, sequence variant of asxl1, and Sjögren syndrome: A case report
Only proven pathogenic mutations associated with myeloid neoplasms are key to establish the clonal nature of the bone marrow fibrosis. In cases with genetic variants of uncertain meaning, the clinical picture may be required to rule out secondary causes.
Enregistré dans:
| Publié dans: | Clin Case Rep |
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| Auteurs principaux: | , , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
John Wiley and Sons Inc.
2020
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7364095/ https://ncbi.nlm.nih.gov/pubmed/32695373 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.2813 |
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