Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect

Nature Genetics

Volumn 37, Issue 12, 2005, Pages 1341-1344

  Monsuur, Alienke J ^a   Bakker, Paul I W De ^b,c   Alizadeh, Behrooz Z ^a   Zhernakova, Alexandra ^a   Bevova, Marianna R ^a   Strengman, Eric ^a   Franke, Lude ^a   Slot, Ruben Van't ^a   Belzen, Martine J Van ^a,e   Lavrijsen, Ineke C M ^a   Diosdado, Begoña ^a   Daly, Mark J ^b,c   Mulder, Chris J J ^d   Mearin, M Luisa ^d,e   Meijer, Jos W R ^f   Meijer, Gerrit A ^d   Oort, Erica Van ^a   Wapenaar, Martin C ^a   Koeleman, Bobby P C ^a   Wijmenga, Cisca ^a  

^a UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^b BROAD INSTITUTE OF MIT AND HARVARD   (United States)

^c MASSACHUSETTS GENERAL HOSPITAL   (United States)

^d VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^e LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^f RIJNSTATE HOSPITAL   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIN; GLUTEN; MYOSIN; MYOSIN 9 B; MYOSIN SUBFRAGMENT; UNCLASSIFIED DRUG;

ACTIN MYOSIN INTERACTION; ARTICLE; CELIAC DISEASE; CONTROLLED STUDY; GENE CLUSTER; GENE LOCATION; GENE REPLICATION; GENETIC ASSOCIATION; GENETIC RISK; GENETIC TRAIT; GENETIC VARIABILITY; HERITABILITY; HUMAN; INTESTINE CELL; INTRON; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RISK ASSESSMENT; SMALL INTESTINE MUCOSA;

AMINO ACID SEQUENCE; CELIAC DISEASE; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; INTESTINE, SMALL; INTRONS; MALE; MOLECULAR SEQUENCE DATA; MYOSINS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 28444452580     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng1680     Document Type: Article

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