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Novel causative variants of VEXAS in UBA1 detected through whole genome transcriptome sequencing in a large cohort of hematological malignancies
UBA1 is an X-linked gene and encodes an ubiquitin-activating enzyme. Three somatic mutations altering the alternative start codon (M41) in UBA1 in hematopoietic precursor cells have recently been described, resulting in a syndrome of severe inflammation, cytopenias, and the presence of intracellular...
Autores principales: | Sakuma, Maki, Blombery, Piers, Meggendorfer, Manja, Haferlach, Claudia, Lindauer, Markus, Martens, Uwe M., Kern, Wolfgang, Haferlach, Torsten, Walter, Wencke |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10169658/ https://www.ncbi.nlm.nih.gov/pubmed/36823397 http://dx.doi.org/10.1038/s41375-023-01857-5 |
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