Somatic Mutations in UBA1 Define a Distinct Subset of Relapsing Polychondritis Patients With VEXAS.

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Title: Somatic Mutations in UBA1 Define a Distinct Subset of Relapsing Polychondritis Patients With VEXAS.
Authors: Ferrada MA; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Sikora KA; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Luo Y; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Wells KV; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Patel B; National Heart, Lung, and Blood Institute, NIH, Bethesda, Maryland., Groarke EM; National Heart, Lung, and Blood Institute, NIH, Bethesda, Maryland., Ospina Cardona D; National Human Genome Research Institute, NIH, Bethesda, Maryland., Rominger E; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Hoffmann P; National Human Genome Research Institute, NIH, Bethesda, Maryland., Le MT; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Deng Z; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Quinn KA; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Rose E; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Tsai WL; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Wigerblad G; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Goodspeed W; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Jones A; National Human Genome Research Institute, NIH, Bethesda, Maryland., Wilson L; National Human Genome Research Institute, NIH, Bethesda, Maryland., Schnappauf O; National Human Genome Research Institute, NIH, Bethesda, Maryland., Laird RS; National Human Genome Research Institute, NIH, Bethesda, Maryland., Kim J; National Institute on Deafness and Other Communication Disorders, NIH, Bethesda, Maryland., Allen C; National Institute on Deafness and Other Communication Disorders, NIH, Bethesda, Maryland., Sirajuddin A; National Heart, Lung, and Blood Institute, NIH, Bethesda, Maryland., Chen M; National Heart, Lung, and Blood Institute, NIH, Bethesda, Maryland., Gadina M; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Calvo KR; NIH Clinical Center, NIH, Bethesda, Maryland., Kaplan MJ; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Colbert RA; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland., Aksentijevich I; National Human Genome Research Institute, NIH, Bethesda, Maryland., Young NS; National Heart, Lung, and Blood Institute, NIH, Bethesda, Maryland., Savic S; NIHR Leeds Biomedical Research Centre of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, UK., Kastner DL; National Human Genome Research Institute, NIH, Bethesda, Maryland., Ombrello AK; National Human Genome Research Institute, NIH, Bethesda, Maryland., Beck DB; National Human Genome Research Institute, NIH, Bethesda, Maryland., Grayson PC; National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland.
Source: Arthritis & rheumatology (Hoboken, N.J.) [Arthritis Rheumatol] 2021 Oct; Vol. 73 (10), pp. 1886-1895. Date of Electronic Publication: 2021 Aug 31.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 101623795 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2326-5205 (Electronic) Linking ISSN: 23265191 NLM ISO Abbreviation: Arthritis Rheumatol Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:2326-5205
DOI:10.1002/art.41743