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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.

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Détails bibliographiques
Publié dans:Clin Case Rep
Auteurs principaux: Santaliestra, Marta, Bussaglia, Elena, Pratcorona, Marta, Monter‐Rovira, Anna, Saavedra, Silvana, Mozos, Anna, Martínez, Clara, Nomdedéu, Josep F.
Format: Artigo
Langue:Inglês
Publié: John Wiley and Sons Inc. 2020
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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