Ultra-rare genetic variation in relapsing polychondritis: a whole-exome sequencing study

Luo, Y., Ferrada, M. A., Sikora, K. A., Rankin, C., Alessi, H. D., Kastner, D. L., Deng, Z., Zhang, M., Merkel, P. A., Kraus, V. B., Allen, A. S., & Grayson, P. C. (2023). Ultra-rare genetic variation in relapsing polychondritis: a whole-exome sequencing study. Annals of the Rheumatic Diseases, 83(2), 253–260. https://doi.org/10.1136/ard-2023-224732
Authors:
Yiming Luo
Marcela A Ferrada
Keith A Sikora
Cameron Rankin
Hugh D Alessi
Daniel L Kastner
Zuoming Deng
Mengqi Zhang
Peter A Merkel
Virginia B Kraus
Andrew S Allen
Peter C Grayson
Affiliated Authors:
Yiming Luo
Columbia Affiliation:
Subjects:
Relapsing Polychondritis and VEXAS Syndrome Research (OpenAlex Topic)
Platelet Disorders and Thrombosis Mechanisms (OpenAlex Topic)
Hereditary Angioedema: Molecular Mechanisms and Clinical Management (OpenAlex Topic)
Genetic Variation (MeSH)
Polychondritis, Relapsing (MeSH)
Author Keywords:
epidemiology
exome sequencing
systemic vasculitis
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Publication Type:
Article
Unique ID:
10.1136/ard-2023-224732
PMID:
37918895
DOI:
10.1136/ard-2023-224732
Journal:
Annals of the Rheumatic Diseases
Publication Date:
Data Source:
PubMed
Source Link:
View PubMed Record
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Record Created: