Associated Papers
Clinical characteristics and genotype analysis of a Chinese patient with juvenile arthritis due to novel LACC1 frameshift mutation and literature review.
Wu Y et al.
Molecular Genetics & Genomic Medicine, 2023
A novel loss-of-function mutation in LACC1 underlies hereditary juvenile arthritis with extended intra-familial phenotypic heterogeneity.
Butbul Aviel Y et al.
Rheumatology (oxford, England), 2021
New or vanishing frontiers: LACC1-associated juvenile arthritis.
Al-Mayouf SM et al.
International Journal of Pediatrics & Adolescent Medicine, 2021
Spectrum of Systemic Auto-Inflammatory Diseases in India: A Multi-Centric Experience.
Suri D et al.
Frontiers in Immunology, 2021
LACC1 gene mutation in three sisters with polyarthritis without systemic features.
Singh A et al.
Annals of the Rheumatic Diseases, 2020
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