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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Detalhes bibliográficos
Publicado no:Clin Case Rep
Main Authors: Santaliestra, Marta, Bussaglia, Elena, Pratcorona, Marta, Monter‐Rovira, Anna, Saavedra, Silvana, Mozos, Anna, Martínez, Clara, Nomdedéu, Josep F.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
Assuntos:
Case Reports
Acesso em linha: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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