Variant mannose-binding lectin alleles are associated with celiac disease

Immunogenetics

Volumn 54, Issue 8, 2002, Pages 596-598

  Boniotto, Michele ^a   Braida, Laura ^a   Spanò, Andrea ^a   Pirulli, Doroti ^a   Baldas, Valentina ^a   Trevisiol, Chiara ^a   Not, Tarcisio ^a,b   Tommasini, Alberto ^b   Amoroso, Antonio ^a,b   Crovella, Sergio ^a,b  

^a UNIVERSITY OF TRIESTE   (Italy)

^b INSTITUTE FOR MATERNAL AND CHILD HEALTH IRCCS BURLO GAROFOLO   (Italy)

Author keywords

Apoptosis; Autoimmunity; Celiac disease; MBL2 polymorphisms

Indexed keywords

LECTIN; MANNOSE BINDING PROTEIN;

ALLELE; ARTICLE; BIOPSY TECHNIQUE; CELIAC DISEASE; CONTROLLED STUDY; DISEASE ASSOCIATION; EXON; GENE FREQUENCY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MUTATION RATE; POINT MUTATION; PRIORITY JOURNAL; PROTEIN VARIANT;

ALLELES; CELIAC DISEASE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; MANNOSE-BINDING LECTIN; POINT MUTATION;

EID: 18744413233     PISSN: 00937711     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00251-002-0504-2     Document Type: Article

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