HLA-Cw*1602: A new susceptibility marker of Behcet's disease in southern Spain

Tissue Antigens

Volumn 51, Issue 1, 1998, Pages 111-114

  Sanz, L ^a   Gonzalez Escribano F ^b   De Pablo, R ^a   Nunez Roldan A ^b   Kreisler, M ^a   Vilches, C ^a  

^a HOSPITAL UNIVERSITARIO PUERTA DE HIERRO   (Spain)

^b HOSPITAL UNIVERSITARIO VIRGEN DEL ROCÍO   (Spain)

Author keywords

B*5108; B51; Behcet's disease; Cw*1602; HLA C; PCR SSP

Indexed keywords

HLA C ANTIGEN; BIOLOGICAL MARKER; MAGEA1 PROTEIN, HUMAN; TUMOR ANTIGEN; TUMOR PROTEIN;

ARTICLE; BEHCET DISEASE; CONTROLLED STUDY; GENE FREQUENCY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENOTYPE; HAPLOTYPE; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MARKER GENE; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM; SPAIN; ALLELE; DISEASE PREDISPOSITION; GENE LINKAGE DISEQUILIBRIUM; GENETIC PREDISPOSITION; GENETICS; IMMUNOLOGY;

ALLELES; ANTIGENS, NEOPLASM; BEHCET SYNDROME; BIOLOGICAL MARKERS; DISEASE SUSCEPTIBILITY; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LINKAGE DISEQUILIBRIUM; NEOPLASM PROTEINS; SPAIN;

EID: 0031594219     PISSN: 00012815     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0039.1998.tb02955.x     Document Type: Article

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