Poulter and colleagues describe a series from the United Kingdom of 10 male patients with VEXAS syndrome, including 2 with novel genetic changes affecting methionine 41 of E1.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8462400PMC
http://dx.doi.org/10.1182/blood.2020010286DOI Listing

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