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Paper Details

Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis.
Sci Rep
16
2019
/, /FAMIN gene, 13, 330 genes, 6, Cys43Tyrfs, FAMIN, FAMIN gene, FARS2, JIA, Juvenile idiopathic arthritis, LACC1, LACC1/, LACC1/FAMIN deficiency, RF, Rheumatoid Factor, Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis, chromosomes 3, chronic, symmetric and erosive arthritis, gene defect, homozygous regions, inflammatory joint disease, patients, polyarticular JIA, rheumatic disease, rheumatoid factor, systemic-onset JIA
Author NameAffiliation
Stephan OssowskiThe Barcelona Institute of Science and Technology
Stephan OssowskiInstitute of Medical Genetics and Applied Genomics, University of Tubingen
Xavier Estivill
Xavier Estivill
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Datasets

Release 1.2