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Paper Details

Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome.
Mol Genet Genomic Med
14
2018
CACP, CACP syndrome, CACP) syndrome, PRG4, PRG4 gene, Patients, Swelling of wrists, knees, and elbows, ascites, autosomal recessive condition, camptodactyly, camptodactyly of hands, camptodactyly-arthropathy-coxa vara-pericarditis (, camptodactyly-arthropathy-coxa vara-pericarditis syndrome, coxa vara, developmental coxa vara, exon 1, familial arthropathic condition, hip involvement, juvenile idiopathic arthritis, modifier gene, noninflammatory arthropathy, patients, pericarditis, pleural effusion, proteoglycan 4, proteoglycan 4 (PRG4) gene, rheumatic diseases
Author NameAffiliation
Mark W YoungbloodYale School of Medicine, Yale University
Kaya BilguvarYale Center for Genome Analysis, Yale School of Medicine
Murat GunelYale School of Medicine, Yale University
Beyhan T??ys??zIstanbul University
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Release 1.2