Genetic dissection between silent and clinically diagnosed symptomatic forms of coeliac disease in multiplex families

Digestive and Liver Disease

Volumn 34, Issue 12, 2002, Pages 842-845

  Mustalahti, K ^a,c   Holopainen, P ^b,c   Karell, K ^b,c   Maki M ^a,c   Partanen, J ^b,c  

^a TAMPERE UNIVERSITY HOSPITAL   (Finland)

^b Finnish Red Cross   (Finland)

^c TAMPERE UNIVERSITY OF TECHNOLOGY   (Finland)

Author keywords

Coeliac disease; HLA DR DQ gene

Indexed keywords

AUTOANTIBODY; HLA DQ ANTIGEN; HLA DR ANTIGEN;

ALLELE; ARTICLE; CELIAC DISEASE; CLINICAL ARTICLE; COMORBIDITY; CONTROLLED STUDY; FAMILY; FEMALE; GENE LOCUS; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; MALABSORPTION; MALE; MUCOSA INFLAMMATION; ONSET AGE; OUTCOMES RESEARCH; SIBLING; SYMPTOMATOLOGY;

EID: 12244274384     PISSN: 15908658     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1590-8658(02)80253-5     Document Type: Article

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