Biallelic mutations in calcium release activated channel regulator 2A (CRACR2A) cause a primary immunodeficiency disorder

Wu, B, Rice, L, Shrimpton, J et al. (9 more authors) (2021) Biallelic mutations in calcium release activated channel regulator 2A (CRACR2A) cause a primary immunodeficiency disorder. eLife, 10. e72559. ISSN 2050-084X

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Copyright, Publisher and Additional Information: © 2021, Wu et al. This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.
Dates:
  • Accepted: 4 December 2021
  • Published (online): 15 December 2021
  • Published: 15 December 2021
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Medicine (Leeds) > Leeds Institute of Cardiovascular and Metabolic Medicine (LICAMM) > Discovery & Translational Science Dept (Leeds)
The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Medicine (Leeds) > Institute of Rheumatology & Musculoskeletal Medicine (LIRMM) (Leeds) > Inflammatory Arthritis (Leeds)
Funding Information:
FunderGrant number
MRC (Medical Research Council)Not Known
Depositing User: Symplectic Publications
Date Deposited: 04 Jan 2022 12:04
Last Modified: 04 Jan 2022 12:04
Status: Published
Publisher: eLife Sciences Publications
Identification Number: https://doi.org/10.7554/eLife.72559
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