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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.
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7364095/ https://www.ncbi.nlm.nih.gov/pubmed/32695373 http://dx.doi.org/10.1002/ccr3.2813 |