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IL1RN genotype as a risk factor for joint pain in hereditary haemochromatosis?

Walker, E J; Riddell, J.; Rodgers, H. J.; Bassett, M. L.; Wilson, S. R.; Cavanaugh, J. A.

Description

Hereditary haemochromatosis is a genetically determined disease of disrupted iron metabolism caused predominantly by the C282Y mutation in the HFE gene on chromosome 6. If detected early, the symptoms of haemochromatosis can usually be prevented by venesection to remove excess iron and maintain normal iron stores.

dc.contributor.authorWalker, E J
dc.contributor.authorRiddell, J.
dc.contributor.authorRodgers, H. J.
dc.contributor.authorBassett, M. L.
dc.contributor.authorWilson, S. R.
dc.contributor.authorCavanaugh, J. A.
dc.date.accessioned2016-04-06T23:48:55Z
dc.date.available2016-04-06T23:48:55Z
dc.identifier.issn0003-4967
dc.identifier.urihttp://hdl.handle.net/1885/100968
dc.description.abstractHereditary haemochromatosis is a genetically determined disease of disrupted iron metabolism caused predominantly by the C282Y mutation in the HFE gene on chromosome 6. If detected early, the symptoms of haemochromatosis can usually be prevented by venesection to remove excess iron and maintain normal iron stores.
dc.description.sponsorshipWe acknowledge the Private Practice Trust Fund at The Canberra Hospital for financial support and the patients and volunteers who participated in this study.
dc.publisherBMJ Publishing Group
dc.rights© BMJ Publishing Group
dc.sourceAnnals of the Rheumatic Diseases
dc.subjectalleles
dc.subjectarthralgia
dc.subjectcase-control studies
dc.subjectfemale
dc.subjectgenetic predisposition to disease
dc.subjectgenotype
dc.subjecthemochromatosis
dc.subjecthumans
dc.subjectmale
dc.subjectreceptors, interleukin-1
dc.titleIL1RN genotype as a risk factor for joint pain in hereditary haemochromatosis?
dc.typeJournal article
local.description.notesImported from ARIES
local.identifier.citationvolume65
dc.date.issued2006
local.identifier.absfor060405
local.identifier.ariespublicationu3488905xPUB58
local.publisher.urlhttp://www.bmj.com/company/
local.type.statusPublished Version
local.contributor.affiliationWalker, Erin, College of Medicine, Biology and Environment, CMBE John Curtin School of Medical Research, Division of Molecular Medicine, The Australian National University
local.contributor.affiliationRiddell, J, Canberra Hospital, Australia
local.contributor.affiliationRodgers, Helen, College of Medicine, Biology and Environment, CMBE Research School of Population Health, Natl Centre for Epidemiology & Population Health, The Australian National University
local.contributor.affiliationBassett, Mark, College of Medicine, Biology and Environment, CMBE ANU Medical School, ANU Medical School, The Australian National University
local.contributor.affiliationWilson, Susan, College of Physical and Mathematical Sciences, CPMS Mathematical Sciences Institute, Centre for Mathematics and Its Applications, The Australian National University
local.contributor.affiliationCavanaugh, Juleen, College of Medicine, Biology and Environment, CMBE ANU Medical School, ANU Medical School, The Australian National University
local.bibliographicCitation.issue2
local.bibliographicCitation.startpage271
local.bibliographicCitation.lastpage272
local.identifier.doi10.1136/ard.2005.038158
dc.date.updated2016-06-14T08:46:26Z
local.identifier.scopusID2-s2.0-31144453914
CollectionsANU Research Publications

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