Linkage and association study of FcγR polymorphisms in celiac disease

Tissue Antigens

Volumn 73, Issue 1, 2009, Pages 54-58

  Sareneva, I ^a   Koskinen, L L E ^a   Korponay Szabo, I R ^b,c   Kaukinen, K ^d,e   Kurppa, K ^e,f   Ziberna, F ^g   Vatta, S ^g   Not, T ^g   Ventura, A ^g   Adany R ^h   Pocsai, Z ^h   Szeles G ^h   Maki M ^e,f   Saavalainen, P ^a   Einarsdottir, E ^a,i  

^a UNIVERSITY OF HELSINKI   (Finland)

^b HEIM PÁL CHILDREN S HOSPITAL   (Hungary)

^c UNIVERSITY OF DEBRECEN   (Hungary)

^d TAMPERE UNIVERSITY HOSPITAL   (Finland)

^e UNIVERSITY OF TAMPERE MEDICAL SCHOOL   (Finland)

^f TAMPERE UNIVERSITY OF TECHNOLOGY   (Finland)

^g UNIVERSITY OF TRIESTE   (Italy)

^h UNIVERSITY OF DEBRECEN   (Hungary)

ⁱ UNIVERSITY OF HELSINKI   (Finland)

Author keywords

1q21 q24; Celiac disease; Complex disease; Fc RIIa; Fc RIIIa; Genetic association

Indexed keywords

FC RECEPTOR 3A; FC RECEPTOR IIA; IMMUNOGLOBULIN RECEPTOR; UNCLASSIFIED DRUG;

ARTICLE; CELIAC DISEASE; CONTROLLED STUDY; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HAPLOTYPE; HUMAN; HUNGARY; ITALY; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; PROTEIN POLYMORPHISM; SINGLE NUCLEOTIDE POLYMORPHISM;

CASE-CONTROL STUDIES; CELIAC DISEASE; CHROMOSOMES, HUMAN, PAIR 1; EPIDEMIOLOGY, MOLECULAR; FINLAND; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; HUNGARY; ITALY; LINKAGE (GENETICS); POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, IGG;

EID: 58149105344     PISSN: 00012815     EISSN: 13990039     Source Type: Journal    
DOI: 10.1111/j.1399-0039.2008.01179.x     Document Type: Article

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