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. 2023 Oct;203(2):331-335.
doi: 10.1111/bjh.19021. Epub 2023 Aug 15.

S56F UBA1 variant is associated with haematological predominant subtype of VEXAS

Adam Al-Hakim  1 , Austin Kulasekararaj  2 , Mohsen Norouzi  3 , Ruth Medlock  4 , Fraser Patrick  5 , Catherine Cargo  6 , Sinisa Savic  1   7
Affiliations

S56F UBA1 variant is associated with haematological predominant subtype of VEXAS

Adam Al-Hakim et al. Br J Haematol. 2023 Oct.
No abstract available

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References

REFERENCES

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    1. Beck DB, Bodian DL, Shah V, Mirshahi UL, Kim J, Ding Y, et al. Estimated Prevalence and Clinical Manifestations of UBA1 Variants Associated With VEXAS Syndrome in a Clinical Population. JAMA. 2023:329(4):318-324. https://doi.org/10.1001/jama.2022.24836
    1. Ferrada MA, Savic S, Cardona DO, Collins JC, Alessi H, Gutierrez-Rodrigues F, et al. Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis. Blood. 2022;140(13):1496-1506. https://doi.org/10.1182/BLOOD.2022016985
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