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dc.contributor.authorStevenson, Paul
dc.contributor.authorRodins, Karl
dc.contributor.authorSusman, Rachel
dc.date.accessioned2019-09-25T01:33:00Z
dc.date.available2019-09-25T01:33:00Z
dc.date.issued2018
dc.identifier.issn0004-8380
dc.identifier.doi10.1111/ajd.12782
dc.identifier.urihttp://hdl.handle.net/10072/387719
dc.description.abstractDear Editor, Familial adenomatous polyposis is an autosomal dominant disorder caused by a germline mutation of the tumour suppressor gene adenomatous polyposis coli (APC) located on chromosome 5q22.2. Familial adenomatous polyposis is characterized by the development of hundreds of polyps in the colorectum, typically beginning in the second or third decade of life and eventually progressing to colorectal cancer in nearly all individuals if left untreated.
dc.languageEnglish
dc.language.isoeng
dc.publisherWiley Blackwell
dc.relation.ispartofpagefromE273
dc.relation.ispartofpagetoE274
dc.relation.ispartofissue4
dc.relation.ispartofjournalAustralasian Journal of Dermatology
dc.relation.ispartofvolume59
dc.subject.fieldofresearchClinical Sciences
dc.subject.fieldofresearchPaediatrics and Reproductive Medicine
dc.subject.fieldofresearchcode1103
dc.subject.fieldofresearchcode1114
dc.subject.keywordsScience & Technology
dc.subject.keywordsLife Sciences & Biomedicine
dc.subject.keywordsDermatology
dc.subject.keywordsGARDNERS-SYNDROME
dc.subject.keywordsPILOMATRICOMAS
dc.titleThe association between multiple pilomatrixomas and APC gene mutations
dc.typeJournal article
dc.type.descriptionC3 - Articles (Letter/ Note)
dcterms.bibliographicCitationStevenson, P; Rodins, K; Susman, R, The association between multiple pilomatrixomas and APC gene mutations, Australasian Journal of Dermatology, 2018, 59 (4), pp. E273-E274
dc.date.updated2019-09-25T01:31:19Z
gro.hasfulltextNo Full Text
gro.griffith.authorStevenson, Paul H.


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