Brief Report: Deficiency of Complement 1r Subcomponent in Early-Onset Systemic Lupus Erythematosus: The Role of Disease-Modifying Alleles in a Monogenic Disease

Arthritis and Rheumatology

Volumn 69, Issue 9, 2017, Pages 1832-1839

  Demirkaya, Erkan ^a   Zhou, Qing ^a,b   Smith, Carolyne K ^c   Ombrello, Michael J ^c   Deuitch, Natalie ^a   Tsai, Wanxia L ^c   Hoffmann, Patrycja ^a   Remmers, Elaine F ^a   Takeuchi, Masaki ^a   Park, Yong Hwan ^a   Chae, JaeJin ^a   Barut, Kenan ^d   Simsek, Dogan ^e   Adrovic, Amra ^d   Sahin, Sezgin ^d   Caliskan, Salim ^d   Chandrasekharappa, Settara C ^a   Hasni, Sarfaraz A ^c   Ombrello, Amanda K ^a   Gadina, Massimo ^c   Kastner, Daniel L ^a   Kaplan, Mariana J ^c   Kasapcopur, Ozgur ^d   Aksentijevich, Ivona ^a   more..

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b ZHEJIANG UNIVERSITY   (China)

^c NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES   (United States)

^d ISTANBUL UNIVERSITY   (Turkey)

^e Universtiy of Health Sciences Gülhane Education and Research Hospital   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

AZATHIOPRINE; COMPLEMENT COMPONENT C1Q; COMPLEMENT COMPONENT C1R; CYCLOPHOSPHAMIDE; HYDROXYCHLOROQUINE; IMMUNOGLOBULIN G; INTERFERON; METHYLPREDNISOLONE;

ADOLESCENT; APHTHOUS STOMATITIS; ARTICLE; CASE REPORT; CELL DENSITY; CHILD; CLINICAL ARTICLE; COGNITIVE DEFECT; CONTROLLED STUDY; CROSS-SECTIONAL STUDY; DISCOID LUPUS ERYTHEMATOSUS; DISEASE SEVERITY; DNA SEQUENCE; ENZYME BLOOD LEVEL; ENZYME DEFICIENCY; EXTRACELLULAR TRAP; FEMALE; FEVER; GENE IDENTIFICATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GRANULOCYTE; HAIR LOSS; HLA SYSTEM; HOMOZYGOTE; HUMAN; HUMAN CELL; INTRACRANIAL HYPERTENSION; LOSS OF FUNCTION MUTATION; LYMPHADENOPATHY; MALE; NEPHRITIS; NEUTROPHIL; PATHOGENESIS; PERIPHERAL BLOOD MONONUCLEAR CELL; PHOTOPHOBIA; PHOTOSENSITIVITY; PRIORITY JOURNAL; PROLIFERATIVE GLOMERULONEPHRITIS; PROTEINURIA; RASH; SANGER SEQUENCING; SCHOOL CHILD; SINGLE NUCLEOTIDE POLYMORPHISM; SJOEGREN SYNDROME; SYSTEMIC LUPUS ERYTHEMATOSUS; TURK (PEOPLE); WEIGHT REDUCTION; WHOLE EXOME SEQUENCING; XEROPHTHALMIA; ADULT; ALLELE; BLOOD; CONSANGUINITY; CYTOLOGY; DEFICIENCY; EXOME; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; METABOLISM; MONONUCLEAR CELL; ONSET AGE; PHENOTYPE; PRESCHOOL CHILD; PROCEDURES; SEVERITY OF ILLNESS INDEX; TURKEY;

ADOLESCENT; ADULT; AGE OF ONSET; ALLELES; CHILD; CHILD, PRESCHOOL; COMPLEMENT C1R; CONSANGUINITY; EXOME; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; INTERFERON TYPE I; LEUKOCYTES, MONONUCLEAR; LUPUS ERYTHEMATOSUS, SYSTEMIC; MALE; NEUTROPHILS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE ANALYSIS, DNA; SEVERITY OF ILLNESS INDEX; TURKEY;

EID: 85022326127     PISSN: 23265191     EISSN: 23265205     Source Type: Journal    
DOI: 10.1002/art.40158     Document Type: Article

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