Monogenic variants in Laccase domain-containing 1 (LACC1) as the cause of juvenile arthritis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Rheumatology
Link
https://link.springer.com/content/pdf/10.1007/s00393-023-01442-2.pdf
Reference29 articles.
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3. Wong SH, Hill AV, Vannberg FO, India-Africa-United Kingdom Leprosy Genetics, C (2010) Genomewide association study of leprosy. N Engl J Med 362:1446–1447. https://doi.org/10.1056/NEJMc1001451 (author reply 1447–1448)
4. Xiong JH et al (2016) Association between genetic variants in NOD2, C13orf31, and CCDC122 genes and leprosy among the Chinese Yi population. Int J Dermatol 55:65–69. https://doi.org/10.1111/ijd.12981
5. Wang D et al (2018) Missense variants in HIF1A and LACC1 contribute to leprosy risk in Han Chinese. Am J Hum Genet 102:794–805. https://doi.org/10.1016/j.ajhg.2018.03.006
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