Gene copy-number variations (CNVs) of complement C4 and C4A deficiency in genetic risk and pathogenesis of juvenile dermatomyositis - Lintner, Katherine E; Patwardhan, Anjali; Rider, Lisa G; Abdul-Aziz, Rabheh; Wu, Yee Ling; Lundström, Emeli; Padyukov, Leonid; Zhou, Bi; Alhomosh, Alaaedin; Newsom, David; White, Peter; Jones, Karla B; et al. (Annals of the rheumatic diseases, 2016)
Keywords: Adolescent; Antigens; Biopsy; Case-Control Studies; Child; Child, Preschool; Complement C4 - deficiency; Complement C4 - genetics; Complement C4a - deficiency; Complement C4a - genetics; Complement C4b - genetics; Dermatomyositis - genetics; Disease; DNA Copy Number Variations; Female; Genes; Genetic Predisposition to Disease; Genomes; Genotype; Haplotypes; Health risk assessment; Hereditary Complement Deficiency Diseases; HLA-DRB1 Chains - genetics; Humans; Immunologic Deficiency Syndromes - genetics; Male; Pathogenesis; Receptors, Tumor Necrosis Factor, Member 25 - blood; Receptors, Tumor Necrosis Factor, Member 25 - genetics; Risk Factors; Tumor necrosis factor-TNF; White people; White People - genetics; United States--US; Gene Polymorphism; Disease Activity; Epidemiology; Autoimmune Diseases; Dermatomyositis