Lack of association of MYO9B genetic variants with coeliac disease in a British cohort

Gut

Volumn 55, Issue 7, 2006, Pages 969-972

  Hunt, K A ^a   Monsuur, A J ^c   McArdle, W L ^d   Kumar, P J ^e   Travis, S P L ^f   Walters, J R F ^b   Jewell, D P ^f   Strachan, D P ^g   Playford, R J ^a   Wijmenga, C ^c   Van Heel, D A ^a  

^a QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

^b IMPERIAL COLLEGE LONDON   (United Kingdom)

^c UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^d UNIVERSITY OF BRISTOL   (United Kingdom)

^e BARTS HEALTH NHS TRUST   (United Kingdom)

^f JOHN RADCLIFFE HOSPITAL   (United Kingdom)

^g ST GEORGE'S UNIVERSITY OF LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIGEN; GUANOSINE TRIPHOSPHATASE ACTIVATING PROTEIN; MYOSIN; PROTEIN MYO 9 B; RHO FACTOR; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ARTICLE; CAUCASIAN; COHORT ANALYSIS; CONTROLLED STUDY; CYTOSKELETON; DNA POLYMORPHISM; EPITHELIUM CELL; ETHNOLOGY; FEMALE; GENE FREQUENCY; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MEMBRANE PERMEABILITY; NETHERLANDS; PRIORITY JOURNAL; SMALL INTESTINE DISEASE; UNITED KINGDOM;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CASE-CONTROL STUDIES; CELIAC DISEASE; CHI-SQUARE DISTRIBUTION; CHILD; CHILD, PRESCHOOL; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GREAT BRITAIN; HAPLOTYPES; HUMANS; MALE; MIDDLE AGED; MYOSINS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 33646574535     PISSN: 00175749     EISSN: None     Source Type: Journal    
DOI: 10.1136/gut.2005.086769     Document Type: Article

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