Items where authors include "Collins, JC"

Article

Ferrada, MA, Savic, S orcid.org/0000-0001-7910-0554, Ospina Cardona, D et al. (29 more authors) (2022) Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis. Blood, 140 (13). pp. 1496-1506. ISSN 0006-4971

Poulter, JA orcid.org/0000-0003-2048-5693, Collins, JC, Cargo, C et al. (12 more authors) (2021) Novel somatic mutations in UBA1 as a cause of VEXAS syndrome. Blood. ISSN 0006-4971

Beck, DB, Ferrada, MA, Sikora, KA et al. (59 more authors) (2020) Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease. New England Journal of Medicine. NEJMoa2026834. ISSN 0028-4793