Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with in...
Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease
About this item
Full title
Author / Creator
Robinson, Philip C , Leo, Paul J , Pointon, Jennifer J , Harris, Jessica , Cremin, Katie , Bradbury, Linda A , Stebbings, Simon , Harrison, Andrew A , Duncan, Emma L , Evans, David M , Wordsworth, Paul B , Brown, Matthew A , Management Committee , Data and Analysis Group , DNA, Genotyping, Data QC and Informatics Group , Wellcome Trust Case Control Consortium , Australian Osteoporosis Genetics Consortium and Publications Committee
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
Formats
Publication information
Publisher
London: Nature Publishing Group UK
Subjects
More information
Scope and Contents
Contents
Ankylosing spondylitis (AS) is a common chronic immune-mediated arthropathy affecting primarily the spine and pelvis. The condition is strongly associated with
HLA-B*27
as well as other human leukocyte antigen variants and at least 47 individual non-MHC-associated variants. However, substantial additional heritability remains as yet unexplain...
Alternative Titles
Full title
Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease
Authors, Artists and Contributors
Author / Creator
Leo, Paul J
Pointon, Jennifer J
Harris, Jessica
Cremin, Katie
Bradbury, Linda A
Stebbings, Simon
Harrison, Andrew A
Duncan, Emma L
Evans, David M
Wordsworth, Paul B
Brown, Matthew A
Management Committee
Data and Analysis Group
DNA, Genotyping, Data QC and Informatics Group
Wellcome Trust Case Control Consortium
Australian Osteoporosis Genetics Consortium
Publications Committee
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5685324
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5685324
Other Identifiers
ISSN
2056-7944
E-ISSN
2056-7944
DOI
10.1038/npjgenmed.2016.8
