Associated Papers
[Monogenic variants in Laccase domain-containing 1 (LACC1) as the cause of juvenile arthritis].
Knieper AM et al.
Zeitschrift Fur Rheumatologie, 2024
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
LACC1 deficiency links juvenile arthritis with autophagy and metabolism in macrophages.
Omarjee O et al.
The Journal of Experimental Medicine, 2021
New or vanishing frontiers: LACC1-associated juvenile arthritis.
Al-Mayouf SM et al.
International Journal of Pediatrics & Adolescent Medicine, 2021
LACC1 gene mutation in three sisters with polyarthritis without systemic features.
Singh A et al.
Annals of the Rheumatic Diseases, 2020
FAMIN Is a Multifunctional Purine Enzyme Enabling the Purine Nucleotide Cycle.
Cader MZ et al.
Cell, 2020
31978345 (PubMed )
Supplement: mmc1.pdf
Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis.
Rabionet R et al.
Scientific Reports, 2019
LACC1 Gene Defects in Familial Form of Juvenile Arthritis.
Karacan I et al.
The Journal of Rheumatology, 2018
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