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Volumn 57, Issue 4, 2008, Pages 463-467

Associations with tight junction genes PARD3 and MAGI2 in Dutch patients point to a common barrier defect for coeliac disease and ulcerative colitis

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CELIAC DISEASE; CONFIDENCE INTERVAL; CONTROLLED STUDY; DATA ANALYSIS; ENTERITIS; GENE; GENE REPLICATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC SCREENING; GENETIC VARIABILITY; HUMAN; INTESTINE EPITHELIUM; INTESTINE MUCOSA PERMEABILITY; MAGI2 GENE; MAJOR CLINICAL STUDY; NETHERLANDS; PARD3 GENE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL SIGNIFICANCE; TIGHT JUNCTION; ULCERATIVE COLITIS; CLINICAL TRIAL; COHORT ANALYSIS; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; METHODOLOGY; MULTICENTER STUDY; PATHOPHYSIOLOGY;

EID: 41149135384     PISSN: 00175749     EISSN: None     Source Type: Journal    
DOI: 10.1136/gut.2007.133132     Document Type: Article
Times cited : (142)

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