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.

Detalles Bibliográficos
Autores principales: Santaliestra, Marta, Bussaglia, Elena, Pratcorona, Marta, Monter‐Rovira, Anna, Saavedra, Silvana, Mozos, Anna, Martínez, Clara, Nomdedéu, Josep F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Case Reports
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

Internet

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

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